A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3486905



Internal ID18727860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1658508..1757404hg38UCSC Ensembl
Innerchr10:1700702..1799598hg19UCSC Ensembl
Innerchr10:1690702..1789598hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3898897
hg1998897
hg1898897
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1042322
Supporting Variants
Samples
Known GenesADARB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3486905
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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