A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027442



Internal ID19116661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134541075..134574490hg38UCSC Ensembl
Innerchr7:134225827..134259242hg19UCSC Ensembl
Innerchr7:133876367..133909782hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3833416
hg1933416
hg1833416
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6636n100
Supporting Variantsnssv3663479
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)nsv1027442
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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