A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037099



Internal ID20604139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6157786..6166656hg38UCSC Ensembl
chr17:6061106..6069976hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg388871
hg198871
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510188
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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