A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017357



Internal ID18759892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72532208..72853910hg38UCSC Ensembl
Innerchr7:71997193..72324490hg19UCSC Ensembl
Innerchr7:71635129..71962426hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38321703
hg19327298
hg18327298
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6459n100
Supporting Variantsnssv3755315
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)nsv1017357
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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