A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355219



Internal ID21012772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:69989414..69995844hg38UCSC Ensembl
chr2:70216546..70222976hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg386431
hg196431
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088910
Samples
Known GenesPCBP1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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