A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16959231



Internal ID40135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:172658090..172658407hg38UCSC Ensembl
chr4:173579241..173579558hg19UCSC Ensembl
Cytoband4q34.1
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6140363
Supporting Variants
Samples
Known GenesGALNTL6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv16959231
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.000312


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