A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363929



Internal ID21021482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148157401..148162900hg38UCSC Ensembl
chr3:147875188..147880687hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg385500
hg195500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096005
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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