A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3501911



Internal ID18800192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4232203..4248812hg38UCSC Ensembl
Innerchr10:4274395..4291004hg19UCSC Ensembl
Innerchr10:4264395..4281004hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3816610
hg1916610
hg1816610
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051538
Supporting Variants
Samples
Known GenesLINC00702
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3501911
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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