A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6365306



Internal ID21022859
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:48429601..48926800hg38UCSC Ensembl
chr3:48471010..48964233hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg38497200
hg19493224
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18209336
Samples
Known GenesARIH2, ARIH2OS, ATRIP, CCDC51, CELSR3, COL7A1, IP6K2, MIR4793, MIR6823, MIR6824, MIR711, NCKIPSD, PFKFB4, PLXNB1, PRKAR2A, SHISA5, SLC25A20, SLC26A6, TMA7, TMEM89, TREX1, UCN2, UQCRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6365306
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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