A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17422422



Internal ID22480292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154355654..154355719hg38UCSC Ensembl
chr5:153735214..153735279hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5891391
Supporting Variants
Samples
Known GenesGALNT10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17422422
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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