A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033137



Internal ID19122359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:65114777..65210761hg38UCSC Ensembl
Innerchr6:65824670..65920654hg19UCSC Ensembl
Innerchr6:65881391..65977375hg18UCSC Ensembl
Cytoband6q12
Allele length
AssemblyAllele length
hg3895985
hg1995985
hg1895985
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6000n100
Supporting Variantsnssv3657664, nssv3657667, nssv3657666, nssv3657665
Samples
Known GenesEYS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033137
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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