A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv756255



Internal ID16050211
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:106190953..106191741hg38UCSC Ensembl
Innerchr10:107950711..107951499hg19UCSC Ensembl
Innerchr10:107940701..107941489hg18UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38789
hg19789
hg18789
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv552105
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)nssv756255
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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