A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340596



Internal ID20998149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:9205201..9207700hg38UCSC Ensembl
chr2:9345330..9347829hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18210718
Samples
Known GenesASAP2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340596
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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