A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017198



Internal ID19106415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:29631090..29737243hg38UCSC Ensembl
Innerchr7:29670706..29776859hg19UCSC Ensembl
Innerchr7:29637231..29743384hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38106154
hg19106154
hg18106154
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6313n100
Supporting Variantsnssv3643337
Samples
Known GenesDPY19L2P3, LOC646762, MIR550A3, ZNRF2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017198
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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