A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321465



Internal ID20854570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:26433986..26436002hg38UCSC Ensembl
chr1:26760477..26762493hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg382017
hg192017
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203473
Samples
Known GenesDHDDS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321465
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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