A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049931



Internal ID18792462
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:90324175..90845607hg38UCSC Ensembl
Innerchr10:92083932..92605364hg19UCSC Ensembl
Innerchr10:92073912..92595344hg18UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38521433
hg19521433
hg18521433
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv952n100
Supporting Variantsnssv3520251, nssv3521657
Samples
Known GenesHTR7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1049931
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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