A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329475



Internal ID20862627
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:86509601..86576600hg38UCSC Ensembl
chr1:86975284..87042283hg19UCSC Ensembl
Cytoband1p22.3
Allele length
AssemblyAllele length
hg3867000
hg1967000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18205179
Samples
Known GenesCLCA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329475
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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