A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169906



Internal ID21313717
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:20530272..20701796hg38UCSC Ensembl
Outerchr17:20527956..20705288hg38UCSC Ensembl
Innerchr17:20433585..20605109hg19UCSC Ensembl
Outerchr17:20431269..20608601hg19UCSC Ensembl
Innerchr17:20374177..20545701hg18UCSC Ensembl
Outerchr17:20371861..20549193hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38177333
hg19177333
hg18177333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14252262
SamplesSNI_6
Known GenesCDRT15L2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169906
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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