A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6336254



Internal ID20993807
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:91425401..91470300hg38UCSC Ensembl
chr2:90396469..90440842hg19UCSC Ensembl
Cytoband2p11.2
Allele length
AssemblyAllele length
hg3844900
hg1944374
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4051n223
Supporting Variantsnssv18210681
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6336254
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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