A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342128



Internal ID20999681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19200219..20084308hg38UCSC Ensembl
chr2:19399980..20284069hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg38884090
hg19884090
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205440
Samples
Known GenesLAPTM4A, LINC00954, MATN3, MIR4757, OSR1, TTC32, WDR35
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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