A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361343



Internal ID21018896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:175184037..175198766hg38UCSC Ensembl
chr3:174901827..174916556hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3814730
hg1914730
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098748
Samples
Known GenesNAALADL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361343
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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