A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017873



Internal ID19107090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:57176322..57822624hg38UCSC Ensembl
Innerchr7:57244029..57882330hg19UCSC Ensembl
Innerchr7:57247971..57886272hg18UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38646303
hg19638302
hg18638302
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6369n100
Supporting Variantsnssv3661488
Samples
Known GenesGUSBP10, MIR3147, ZNF716
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017873
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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