A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057435



Internal ID19146654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46120237..46286792hg38UCSC Ensembl
Innerchr17:44197603..44364158hg19UCSC Ensembl
Innerchr17:41553381..41719935hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg38166556
hg19166556
hg18166555
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3195n100
Supporting Variantsnssv3720649, nssv3720647, nssv3720648, nssv3549822
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)nsv1057435
Frequency
Sample Size11257
Observed Gain2
Observed Loss2
Observed Complex0
Frequencyn/a


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