A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065029



Internal ID19154248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:68094944..68178753hg38UCSC Ensembl
Innerchr17:66091085..66174894hg19UCSC Ensembl
Innerchr17:63602722..63686489hg18UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3883810
hg1983810
hg1883768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3277n100
Supporting Variantsnssv3567755, nssv3725148, nssv3725147, nssv3725146, nssv3567756, nssv3567754
Samples
Known GenesLINC00674
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065029
Frequency
Sample Size11257
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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