A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351201



Internal ID21008754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:158832414..159065569hg38UCSC Ensembl
chr2:159688926..159922081hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg38233156
hg19233156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079882
Samples
Known GenesTANC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351201
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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