A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050459



Internal ID19139678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7416409..7435548hg38UCSC Ensembl
Innerchr10:7458371..7477510hg19UCSC Ensembl
Innerchr10:7498377..7517516hg18UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3819140
hg1919140
hg1819140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707682
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)nsv1050459
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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