A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv550325



Internal ID16337734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:29956632..29976164hg38UCSC Ensembl
Innerchr10:30245561..30265093hg19UCSC Ensembl
Innerchr10:30285567..30305099hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3819533
hg1919533
hg1819533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173877
Samples1780854097_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv550325
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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