A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354337



Internal ID21011890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:173810076..173813264hg38UCSC Ensembl
chr2:174674804..174677992hg19UCSC Ensembl
Cytoband2q31.1
Allele length
AssemblyAllele length
hg383189
hg193189
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081351
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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