A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056155



Internal ID18798686
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:46131308..46192180hg38UCSC Ensembl
Innerchr17:44208674..44269546hg19UCSC Ensembl
Innerchr17:41564451..41625323hg18UCSC Ensembl
Cytoband17q21.31
Allele length
AssemblyAllele length
hg3860873
hg1960873
hg1860873
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3210n100
Supporting Variantsnssv3549958, nssv3549959
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)nsv1056155
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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