A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065535



Internal ID19154754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4391668..4457059hg38UCSC Ensembl
Innerchr17:4294963..4360354hg19UCSC Ensembl
Innerchr17:4241712..4307103hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3865392
hg1965392
hg1865392
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3087n100
Supporting Variantsnssv3719154
Samples
Known GenesSPNS3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1065535
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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