A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18149099



Internal ID20716139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:87488104..87492313hg38UCSC Ensembl
chr6:88197822..88202031hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg384210
hg194210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6411360
Supporting Variants
Samples
Known GenesSLC35A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18149099
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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