A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064968



Internal ID18807499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46113306..46190497hg38UCSC Ensembl
Innerchr17:44190672..44267863hg19UCSC Ensembl
Innerchr17:41546454..41623640hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3877192
hg1977192
hg1877187
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3203n100
Supporting Variantsnssv3548630, nssv3548635, nssv3548634, nssv3548632, nssv3548628, nssv3548631, nssv3548629, nssv3548633
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)nsv1064968
Frequency
Sample Size29084
Observed Gain7
Observed Loss1
Observed Complex0
Frequencyn/a


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