A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359147



Internal ID21016700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155141939..155142753hg38UCSC Ensembl
chr3:154859728..154860542hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38815
hg19815
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096398
Samples
Known GenesMME
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359147
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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