A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17619131



Internal ID21811178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7972750..7972859hg38UCSC Ensembl
chr19:8037634..8037743hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38110
hg19110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6042555
Supporting Variants
Samples
Known GenesELAVL1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17619131
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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