A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18036002



Internal ID20603042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:39931648..39932427hg38UCSC Ensembl
chr17:38087901..38088680hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38780
hg19780
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6510103
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18036002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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