A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18177585



Internal ID20744625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:68189892..68214293hg38UCSC Ensembl
chr17:66186033..66210434hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg3824402
hg1924402
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6524354
Supporting Variants
Samples
Known GenesLOC440461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18177585
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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