A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv751858



Internal ID16045814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:80453946..80458916hg38UCSC Ensembl
Innerchr10:82213702..82218672hg19UCSC Ensembl
Innerchr10:82203682..82208652hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg384971
hg194971
hg184971
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv551640
Supporting Variants
Samples
Known GenesTSPAN14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv751858
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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