A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325718



Internal ID20858850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:24743701..24746700hg38UCSC Ensembl
chr1:25070192..25073191hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383000
hg193000
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18201295
Samples
Known GenesCLIC4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325718
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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