A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349771



Internal ID21007324
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:30624801..30632300hg38UCSC Ensembl
chr2:30847667..30855166hg19UCSC Ensembl
Cytoband2p23.1
Allele length
AssemblyAllele length
hg387500
hg197500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085206
Samples
Known GenesLCLAT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349771
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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