A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026859



Internal ID18769390
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134512710..134558688hg38UCSC Ensembl
Innerchr7:134197462..134243440hg19UCSC Ensembl
Innerchr7:133848002..133893980hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3845979
hg1945979
hg1845979
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752530
Samples
Known GenesAKR1B10, AKR1B15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026859
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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