A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3487698



Internal ID18728653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:1393005..1413573hg38UCSC Ensembl
Innerchr10:1435200..1455768hg19UCSC Ensembl
Innerchr10:1425200..1445768hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3820569
hg1920569
hg1820569
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1040045
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)nssv3487698
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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