A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338546



Internal ID20996099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:224624561..224635769hg38UCSC Ensembl
chr2:225489278..225500486hg19UCSC Ensembl
Cytoband2q36.2
Allele length
AssemblyAllele length
hg3811209
hg1911209
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083812
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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