A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1041940



Internal ID19131159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:52861582..52977768hg38UCSC Ensembl
Innerchr10:54621342..54737528hg19UCSC Ensembl
Innerchr10:54291348..54407534hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg38116187
hg19116187
hg18116187
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3508810
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)nsv1041940
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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