A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352628



Internal ID21010181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:8145199..8145487hg38UCSC Ensembl
chr2:8285329..8285617hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090872
Samples
Known GenesLINC00299
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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