A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18037708



Internal ID20604748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:76852920..76855771hg38UCSC Ensembl
chr17:74849002..74851853hg19UCSC Ensembl
Cytoband17q25.2
Allele length
AssemblyAllele length
hg382852
hg192852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6520570
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18037708
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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