A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340192



Internal ID20997745
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:63938765..63983389hg38UCSC Ensembl
chr2:64165899..64210523hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3844625
hg1944625
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089273
Samples
Known GenesVPS54
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340192
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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