A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18057439



Internal ID20624479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:211791718..211792490hg38UCSC Ensembl
chr1:211965060..211965832hg19UCSC Ensembl
Cytoband1q32.3
Allele length
AssemblyAllele length
hg38773
hg19773
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6319299
Supporting Variants
Samples
Known GenesLPGAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18057439
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.03116


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