A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318991



Internal ID20852083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23624918..23628498hg38UCSC Ensembl
chr1:23951408..23954988hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383581
hg193581
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202467
Samples
Known GenesMDS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318991
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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