A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1040758



Internal ID18783289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:34078714..34116395hg38UCSC Ensembl
Innerchr10:34367642..34405323hg19UCSC Ensembl
Innerchr10:34407648..34445329hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3837682
hg1937682
hg1837682
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3506152
Samples
Known GenesPARD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1040758
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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