A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042376



Internal ID19131595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:6628773..6868922hg38UCSC Ensembl
Innerchr10:6670735..6910884hg19UCSC Ensembl
Innerchr10:6710741..6950890hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38240150
hg19240150
hg18240150
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3486971
Samples
Known GenesLINC00706, LINC00707
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042376
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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