A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370376



Internal ID21027929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174068340..174098331hg38UCSC Ensembl
chr3:173786130..173816121hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3829992
hg1929992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097239
Samples
Known GenesNLGN1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370376
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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