A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033492



Internal ID19122713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:13650797..13706829hg38UCSC Ensembl
Innerchr7:13690422..13746454hg19UCSC Ensembl
Innerchr7:13656947..13712979hg18UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3856033
hg1956033
hg1856033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643144, nssv3643145
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)nsv1033492
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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