A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031200



Internal ID19120421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54178364..54218437hg38UCSC Ensembl
Innerchr7:54246057..54286130hg19UCSC Ensembl
Innerchr7:54213551..54253624hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3840074
hg1940074
hg1840074
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661321, nssv3661320
Samples
Known GenesHPVC1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031200
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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