A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349445



Internal ID21006998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:3835906..3876373hg38UCSC Ensembl
chr2:3883496..3923963hg19UCSC Ensembl
Cytoband2p25.3
Allele length
AssemblyAllele length
hg3840468
hg1940468
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086351
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349445
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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