A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032815



Internal ID18775349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16358401..17364877hg38UCSC Ensembl
Innerchr7:16398026..17404501hg19UCSC Ensembl
Innerchr7:16364551..17371026hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg381006477
hg191006476
hg181006476
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6289n100
Supporting Variantsnssv3643199
Samples
Known GenesAGR2, AGR3, AHR, ANKMY2, BZW2, ISPD, LRRC72, SOSTDC1, TSPAN13
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032815
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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