A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035329



Internal ID20602369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39153804..39154488hg38UCSC Ensembl
chr17:37310057..37310741hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38685
hg19685
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6515196
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035329
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00011


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