A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv552174



Internal ID16339583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:111177701..111555882hg38UCSC Ensembl
Innerchr10:112937459..113315640hg19UCSC Ensembl
Innerchr10:112927449..113305630hg18UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg38378182
hg19378182
hg18378182
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv758425
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv552174
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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