A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4010176



Internal ID22071807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20527867..20701796hg38UCSC Ensembl
Outerchr17:20510133..20705288hg38UCSC Ensembl
Innerchr17:20431180..20605109hg19UCSC Ensembl
Outerchr17:20413446..20608601hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38195156
hg19195156
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1155393
Supporting Variants
Samples
Known GenesCDRT15L2
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4010176
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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