A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3720595



Internal ID19018876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46103588..46286792hg38UCSC Ensembl
Innerchr17:44180954..44364158hg19UCSC Ensembl
Innerchr17:41536766..41719935hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38183205
hg19183205
hg18183170
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066484
Supporting Variants
Samples
Known GenesKANSL1, KANSL1-AS1, LOC644172
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3720595
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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