A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv1407e199



Internal ID20124709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:155803573..155984165hg38UCSC Ensembl
chrX:155033236..155213830hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38180593
hg19180595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2664638, esv2670089
SamplesNA19648, NA18621, HG00249, NA19332, HG01066, HG00315, NA19350, NA19057, NA18596, NA19377, NA18606, NA19443, NA12400, NA19067, HG01140, HG00271, NA19107, NA19068, NA18595, NA18619, NA12348, NA19313, HG00139, HG01067, NA18874, HG00232, HG00422, NA18557, NA19445, NA18908, NA18867, HG00419, NA18638, HG00154, NA18544, NA19247, HG00443, NA19462, NA18637, NA18579, NA19064, NA18548, HG00740, NA18566, HG00651, NA19084, NA06989, NA18853, NA19059, HG00152, NA18536, HG00246, NA18576, NA20799, NA18632, HG00155, NA18535, NA18543, NA19434, NA18950, NA19010, NA19835, HG01137, HG00319, NA18610, HG00339, NA19248, NA19472, HG01055, NA18636, NA18873, NA11843, NA18983, NA19004, NA19312, NA18549, NA18487, HG00437, NA20509, NA18620
Known GenesVAMP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)dgv1407e199
Frequency
Sample Size1151
Observed Gain0
Observed Loss80
Observed Complex0
Frequencyn/a


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