A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023714



Internal ID19112931
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:79621532..79661574hg38UCSC Ensembl
Innerchr7:79250848..79290890hg19UCSC Ensembl
Innerchr7:79088784..79128826hg18UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3840043
hg1940043
hg1840043
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3657179
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023714
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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