A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18146149



Internal ID20713189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:91650714..91707911hg38UCSC Ensembl
chr6:92360432..92417629hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3857198
hg1957198
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6409303
Supporting Variants
Samples
Known GenesCASC6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18146149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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