A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033272



Internal ID19122494
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26936807..26980587hg38UCSC Ensembl
Innerchr7:26976426..27020206hg19UCSC Ensembl
Innerchr7:26942951..26986731hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3843781
hg1943781
hg1843781
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643323
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)nsv1033272
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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