A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024477



Internal ID18767009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111019950..111304421hg38UCSC Ensembl
Innerchr7:110660006..110944477hg19UCSC Ensembl
Innerchr7:110447242..110731713hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38284472
hg19284472
hg18284472
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3645219
Samples
Known GenesIMMP2L, LRRN3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024477
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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