A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17715891



Internal ID139557
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:2876497..2876927hg38UCSC Ensembl
chr18:2876495..2876925hg19UCSC Ensembl
Cytoband18p11.32
Allele length
AssemblyAllele length
hg38431
hg19431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6145186
Supporting Variants
Samples
Known GenesEMILIN2
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nssv17715891
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08713


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