A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6350565



Internal ID21008118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30256328..30269484hg38UCSC Ensembl
chr2:30479194..30492350hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg3813157
hg1913157
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208186
Samples
Known GenesLBH
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6350565
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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