A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061197



Internal ID18803728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46130778..46194634hg38UCSC Ensembl
Innerchr17:44208144..44272000hg19UCSC Ensembl
Innerchr17:41563921..41627777hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3863857
hg1963857
hg1863857
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3210n100
Supporting Variantsnssv3720905, nssv3720906
Samples
Known GenesKANSL1, KANSL1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061197
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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