A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9757796



Internal ID18732042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:85254364..85254645hg38UCSC Ensembl
OuterchrX:85254271..85254713hg38UCSC Ensembl
InnerchrX:84509370..84509651hg19UCSC Ensembl
OuterchrX:84509277..84509719hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3559049
Supporting Variants
Samples
Known GenesZNF711
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9757796
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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