A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3516112



Internal ID18467707
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:43236073..43364859hg38UCSC Ensembl
Innerchr10:43731521..43860307hg19UCSC Ensembl
Innerchr10:43051527..43180313hg18UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38128787
hg19128787
hg18128787
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044422
Supporting Variants
Samples
Known GenesRASGEF1A
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3516112
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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