A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031875



Internal ID18774409
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72532208..72854414hg38UCSC Ensembl
Innerchr7:71997193..72324994hg19UCSC Ensembl
Innerchr7:71635129..71962930hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38322207
hg19327802
hg18327802
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6460n100
Supporting Variantsnssv3755316
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031875
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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