A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024493



Internal ID18767025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:33733357..34425137hg38UCSC Ensembl
Innerchr7:33772969..34464749hg19UCSC Ensembl
Innerchr7:33739494..34431274hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38691781
hg19691781
hg18691781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643399
Samples
Known GenesBMPER, NPSR1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024493
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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