A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334619



Internal ID20867806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:159474182..159947925hg38UCSC Ensembl
chr1:159443972..159917715hg19UCSC Ensembl
Cytoband1q23.2
Allele length
AssemblyAllele length
hg38473744
hg19473744
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200967
Samples
Known GenesAPCS, C1orf204, CCDC19, CRP, DUSP23, FCRL6, IGSF9, OR10J5, SLAMF8, TAGLN2, VSIG8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334619
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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