A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055505



Internal ID18798036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46088437..46215377hg38UCSC Ensembl
Innerchr17:44165803..44292743hg19UCSC Ensembl
Innerchr17:41521621..41648520hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38126941
hg19126941
hg18126900
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3182n100
Supporting Variantsnssv3546376, nssv3546378, nssv3546379, nssv3546377, nssv3720318, nssv3546375, nssv3720319, nssv3546374
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)nsv1055505
Frequency
Sample Size29084
Observed Gain8
Observed Loss0
Observed Complex0
Frequencyn/a


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