A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342337



Internal ID20999890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149424764..149425123hg38UCSC Ensembl
chr2:150281278..150281637hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg38360
hg19360
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077792
Samples
Known GenesLYPD6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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