A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2676956



Internal ID9943061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140411591..140420821hg38UCSC Ensembl
chrX:139493756..139502986hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg389231
hg199231
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1402e199
Supporting Variantsessv6258634, essv6095187, essv6571563, essv5978071, essv6420502
SamplesNA19657, HG00275, NA19654, HG00278, HG01191
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2676956
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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