A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3501498



Internal ID19089139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:565930..622203hg38UCSC Ensembl
Innerchr10:611870..668143hg19UCSC Ensembl
Innerchr10:601870..658143hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3856274
hg1956274
hg1856274
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050010
Supporting Variants
Samples
Known GenesDIP2C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3501498
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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