A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18143259



Internal ID20710299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:17408928..17416153hg38UCSC Ensembl
chr6:17409159..17416384hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg387226
hg197226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410595
Supporting Variants
Samples
Known GenesCAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18143259
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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