A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18134601



Internal ID20701641
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:104121263..104276647hg38UCSC Ensembl
chr6:104569138..104724522hg19UCSC Ensembl
Cytoband6q16.3
Allele length
AssemblyAllele length
hg38155385
hg19155385
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610186
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18134601
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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