A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023612



Internal ID18766145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:82592183..83790140hg38UCSC Ensembl
Innerchr7:82221499..83419456hg19UCSC Ensembl
Innerchr7:82059435..83257392hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg381197958
hg191197958
hg181197958
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655154
Samples
Known GenesMIR7976, PCLO, SEMA3E
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023612
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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