A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015980



Internal ID19105198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:118068680..118082066hg38UCSC Ensembl
Innerchr7:117708734..117722120hg19UCSC Ensembl
Innerchr7:117495970..117509356hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3813387
hg1913387
hg1813387
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6593n100
Supporting Variantsnssv3662053
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)nsv1015980
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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