A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323240



Internal ID20856357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:19973897..19975847hg38UCSC Ensembl
chr1:20300390..20302340hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg381951
hg191951
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056562
Samples
Known GenesPLA2G2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323240
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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