A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3663474



Internal ID18615069
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134448868..134482369hg38UCSC Ensembl
Innerchr7:134133620..134167121hg19UCSC Ensembl
Innerchr7:133784160..133817661hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3833502
hg1933502
hg1833502
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023263
Supporting Variants
Samples
Known GenesAKR1B1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3663474
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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