A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3511497



Internal ID18809778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:70352677..70394751hg38UCSC Ensembl
Innerchr10:72112433..72154507hg19UCSC Ensembl
Innerchr10:71782439..71824513hg18UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3842075
hg1942075
hg1842075
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044989
Supporting Variants
Samples
Known GenesLRRC20
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3511497
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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