A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372091



Internal ID21029644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155255469..155382367hg38UCSC Ensembl
chr3:154973258..155100156hg19UCSC Ensembl
Cytoband3q25.2
Allele length
AssemblyAllele length
hg38126899
hg19126899
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096409
Samples
Known GenesLOC100507537
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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