A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3548641



Internal ID18500236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46113306..46192180hg38UCSC Ensembl
Innerchr17:44190672..44269546hg19UCSC Ensembl
Innerchr17:41546454..41625323hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3878875
hg1978875
hg1878870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058973
Supporting Variants
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)nssv3548641
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer