A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352124



Internal ID21009677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:149209042..149209670hg38UCSC Ensembl
chr2:150065556..150066184hg19UCSC Ensembl
Cytoband2q23.2
Allele length
AssemblyAllele length
hg38629
hg19629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077786
Samples
Known GenesLYPD6B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352124
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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