A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028641



Internal ID19117859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15205321..15269734hg38UCSC Ensembl
Innerchr7:15244946..15309359hg19UCSC Ensembl
Innerchr7:15211471..15275884hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3864414
hg1964414
hg1864414
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6286n100
Supporting Variantsnssv3643175
Samples
Known GenesAGMO
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028641
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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