A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044938



Internal ID18787469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:28313064..28370511hg38UCSC Ensembl
Innerchr10:28601993..28659440hg19UCSC Ensembl
Innerchr10:28641999..28699446hg18UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg3857448
hg1957448
hg1857448
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3707746
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)nsv1044938
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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