A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033587



Internal ID19122808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134541075..134575354hg38UCSC Ensembl
Innerchr7:134225827..134260106hg19UCSC Ensembl
Innerchr7:133876367..133910646hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3834280
hg1934280
hg1834280
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6636n100
Supporting Variantsnssv3664223, nssv3663483, nssv3663480, nssv3663482, nssv3664222, nssv3663481
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)nsv1033587
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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