A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv750287



Internal ID15697557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:74332421..74600264hg38UCSC Ensembl
Innerchr10:76092179..76360022hg19UCSC Ensembl
Innerchr10:75762185..76030028hg18UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg38267844
hg19267844
hg18267844
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551528
Supporting Variants
Samples
Known GenesADK
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv750287
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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