A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149094



Internal ID20716134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87429244..87433587hg38UCSC Ensembl
chr6:88138962..88143305hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384344
hg194344
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6397641
Supporting Variants
Samples
Known GenesC6orf165
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149094
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00051


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