A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1048496



Internal ID19137715
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7505226..7539503hg38UCSC Ensembl
Innerchr10:7547188..7581465hg19UCSC Ensembl
Innerchr10:7587194..7621471hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3834278
hg1934278
hg1834278
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3501085
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1048496
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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