A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18035767



Internal ID20602807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:5255908..5268495hg38UCSC Ensembl
chr17:5159203..5171790hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3812588
hg1912588
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6509761
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18035767
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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