A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6020074



Internal ID9674134
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 Flag1
Merged StatusS
Merged Variantsesv2662500
Supporting Variants
SamplesNA19403
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6020074
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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