A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18034085



Internal ID20601125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17195563..17198970hg38UCSC Ensembl
chr17:17098877..17102284hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg383408
hg193408
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6511027
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18034085
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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