A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv551242



Internal ID16338651
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:65197205..65306640hg38UCSC Ensembl
Innerchr10:66956963..67066398hg19UCSC Ensembl
Innerchr10:66626969..66736404hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38109436
hg19109436
hg18109436
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv749370
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv551242
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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