A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372725



Internal ID21030278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183137101..183138800hg38UCSC Ensembl
chr3:182854889..182856588hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098475
Samples
Known GenesLAMP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372725
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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