A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041785



Internal ID19131004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4464966..4522002hg38UCSC Ensembl
Innerchr10:4507158..4564194hg19UCSC Ensembl
Innerchr10:4497158..4554194hg18UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3857037
hg1957037
hg1857037
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3490317, nssv3492935
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)nsv1041785
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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