A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355297



Internal ID21012850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:145552101..145555900hg38UCSC Ensembl
chr2:146309669..146313468hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg383800
hg193800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078827
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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