A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327382



Internal ID20860520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:9474863..9478854hg38UCSC Ensembl
chr1:9534922..9538913hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg383992
hg193992
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203196
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327382
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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