A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1043757



Internal ID19132976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:81488191..81591486hg38UCSC Ensembl
Innerchr10:83247947..83351242hg19UCSC Ensembl
Innerchr10:83237927..83341222hg18UCSC Ensembl
Cytoband10q23.1
Allele length
AssemblyAllele length
hg38103296
hg19103296
hg18103296
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3521374, nssv3503413
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)nsv1043757
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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