A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370963



Internal ID21028516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:59049601..59050200hg38UCSC Ensembl
chr3:59035327..59035926hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103511
Samples
Known GenesC3orf67
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370963
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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