A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662500



Internal ID9928605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:56919015..56930414hg38UCSC Ensembl
chrX:56945448..56956847hg19UCSC Ensembl
CytobandXp11.21
Allele length
AssemblyAllele length
hg3811400
hg1911400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6020074, essv5726359, essv6131942, essv6016848, essv6292959, essv5779729, essv6266699
SamplesNA19701, NA19399, NA18504, NA19379, NA19138, NA19403, NA19625
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662500
Frequency
Sample Size1151
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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