A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327462



Internal ID20860601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:58537186..58537730hg38UCSC Ensembl
chr1:59002858..59003402hg19UCSC Ensembl
Cytoband1p32.1
Allele length
AssemblyAllele length
hg38545
hg19545
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061915
Samples
Known GenesOMA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327462
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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