A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016071



Internal ID19105289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56740039..57053295hg38UCSC Ensembl
Innerchr7:56807732..57121002hg19UCSC Ensembl
Innerchr7:56775226..57124944hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38313257
hg19313271
hg18349719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6366n100
Supporting Variantsnssv3661478, nssv3661477
Samples
Known GenesLOC100130849, MIR4283-1, MIR4283-2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016071
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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