A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062276



Internal ID18804807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46114400..46185584hg38UCSC Ensembl
Innerchr17:44191766..44262950hg19UCSC Ensembl
Innerchr17:41547543..41618727hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3871185
hg1971185
hg1871185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3199n100
Supporting Variantsnssv3549774, nssv3720618
Samples
Known GenesKANSL1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062276
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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