A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033209



Internal ID19122431
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:134542547..134579534hg38UCSC Ensembl
Innerchr7:134227299..134264286hg19UCSC Ensembl
Innerchr7:133877839..133914826hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3836988
hg1936988
hg1836988
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6636n100
Supporting Variantsnssv3664225
Samples
Known GenesAKR1B15
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033209
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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