A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv752138



Internal ID16046094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:83534299..83570318hg38UCSC Ensembl
Innerchr10:85294055..85330074hg19UCSC Ensembl
Innerchr10:85284035..85320054hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg3836020
hg1936020
hg1836020
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551747
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv752138
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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