A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6375137



Internal ID21032690
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:175085378..175089865hg38UCSC Ensembl
chr3:174803168..174807655hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg384488
hg194488
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098740
Samples
Known GenesNAALADL2, NAALADL2-AS3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6375137
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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