A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019032



Internal ID19108249
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:40165007..40240724hg38UCSC Ensembl
Innerchr7:40204606..40280323hg19UCSC Ensembl
Innerchr7:40171131..40246848hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3875718
hg1975718
hg1875718
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643876
Samples
Known GenesC7orf10
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019032
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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