A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18128660



Internal ID20695700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:150777592..150935919hg38UCSC Ensembl
chr5:150157154..150315481hg19UCSC Ensembl
Cytoband5q33.1
Allele length
AssemblyAllele length
hg38158328
hg19158328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6407534
Supporting Variants
Samples
Known GenesIRGM, SMIM3, ZNF300, ZNF300P1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18128660
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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