A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325381



Internal ID20858512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1978801..1981500hg38UCSC Ensembl
chr1:1910240..1912939hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg382700
hg192700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18202320
Samples
Known GenesKIAA1751
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325381
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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