A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349811



Internal ID21007364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:160035618..160036292hg38UCSC Ensembl
chr2:160892129..160892803hg19UCSC Ensembl
Cytoband2q24.2
Allele length
AssemblyAllele length
hg38675
hg19675
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18080516
Samples
Known GenesPLA2R1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349811
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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