A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3559049



Internal ID18760125
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 StatusM
Merged Variants
Supporting Variantsessv9757796
Samples
Known GenesZNF711
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3559049
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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