A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362970



Internal ID21020523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127603052..127603363hg38UCSC Ensembl
chr3:127321895..127322206hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg38312
hg19312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094105
Samples
Known GenesMCM2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362970
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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