A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18140768



Internal ID20707808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:2670997..2676602hg38UCSC Ensembl
chr6:2671231..2676836hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg385606
hg195606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6408070
Supporting Variants
Samples
Known GenesMYLK4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18140768
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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