A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2670089



Internal ID9589508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:155803607..155984130hg38UCSC Ensembl
OuterchrX:155803573..155984165hg38UCSC Ensembl
InnerchrX:155033270..155213795hg19UCSC Ensembl
OuterchrX: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 Variantsdgv1407e199
Supporting Variantsessv6290608
SamplesHG00271
Known GenesVAMP7
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2670089
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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