A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv744735



Internal ID16038691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:25046925..25096929hg38UCSC Ensembl
Innerchr10:25335854..25385858hg19UCSC Ensembl
Innerchr10:25375860..25425864hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3850005
hg1950005
hg1850005
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550224
Supporting Variants
Samples
Known GenesENKUR
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv744735
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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