A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061017



Internal ID18803548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:3595117..3654147hg38UCSC Ensembl
Innerchr17:3498411..3557441hg19UCSC Ensembl
Innerchr17:3445160..3504190hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3859031
hg1959031
hg1859031
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3085n100
Supporting Variantsnssv3560091
Samples
Known GenesCTNS, SHPK, TRPV1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061017
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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