A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010102



Internal ID22071733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:15140609..15151185hg38UCSC Ensembl
Outerchr17:15134796..15155674hg38UCSC Ensembl
Innerchr17:15043926..15054502hg19UCSC Ensembl
Outerchr17:15038113..15058991hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3820879
hg1920879
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155378
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010102
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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