A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321576



Internal ID20854684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:215619683..215672853hg38UCSC Ensembl
chr1:215793025..215846195hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg3853171
hg1953171
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200570
Samples
Known GenesKCTD3, USH2A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321576
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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