A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337900



Internal ID20995453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:4633904..4634319hg38UCSC Ensembl
chr2:4681494..4681909hg19UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg38416
hg19416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089944
Samples
Known GenesLOC727982
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337900
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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