A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756077



Internal ID15703347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:102397954..102410447hg38UCSC Ensembl
Innerchr10:104157711..104170204hg19UCSC Ensembl
Innerchr10:104147701..104160194hg18UCSC Ensembl
Cytoband10q24.32
Allele length
AssemblyAllele length
hg3812494
hg1912494
hg1812494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552058
Supporting Variants
Samples
Known GenesNFKB2, PSD
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv756077
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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