A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373742



Internal ID21031295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:53034382..53041620hg38UCSC Ensembl
chr3:53068398..53075636hg19UCSC Ensembl
Cytoband3p21.1
Allele length
AssemblyAllele length
hg387239
hg197239
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100998
Samples
Known GenesSFMBT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373742
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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