A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6369660



Internal ID9529946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:64785205..64842336hg38UCSC Ensembl
OuterchrX:64785048..64842497hg38UCSC Ensembl
InnerchrX:64005085..64062216hg19UCSC Ensembl
OuterchrX:64004928..64062377hg19UCSC Ensembl
CytobandXq11.2
Allele length
AssemblyAllele length
hg3857450
hg1957450
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2656993
Supporting Variants
SamplesNA19059
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6369660
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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