A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv742192



Internal ID16036148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4662517..4668106hg38UCSC Ensembl
Innerchr10:4704709..4710298hg19UCSC Ensembl
Innerchr10:4694709..4700298hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg385590
hg195590
hg185590
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv549864
Supporting Variants
Samples
Known GenesLINC00704
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv742192
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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