A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034496



Internal ID19123718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13063277..13235917hg38UCSC Ensembl
Innerchr7:13102902..13275542hg19UCSC Ensembl
Innerchr7:13069427..13242067hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38172641
hg19172641
hg18172641
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643036
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)nsv1034496
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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