A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3493970



Internal ID18734925
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:173392..739989hg38UCSC Ensembl
Innerchr10:219332..785929hg19UCSC Ensembl
Innerchr10:209332..775929hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg38566598
hg19566598
hg18566598
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1052660
Supporting Variants
Samples
Known GenesDIP2C, MIR5699, PRR26, ZMYND11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3493970
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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