A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149672



Internal ID20716712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87667692..87673638hg38UCSC Ensembl
chr6:88377410..88383356hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg385947
hg195947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408696
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149672
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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