A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015823



Internal ID19105041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:27272182..27300780hg38UCSC Ensembl
Innerchr7:27311801..27340399hg19UCSC Ensembl
Innerchr7:27278326..27306924hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3828599
hg1928599
hg1828599
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643324
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)nsv1015823
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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