A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359862



Internal ID21017415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:183403881..183411880hg38UCSC Ensembl
chr3:183121669..183129668hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg388000
hg198000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098487
Samples
Known GenesMCF2L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359862
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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