A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326950



Internal ID20860087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:6752019..6754758hg38UCSC Ensembl
chr1:6812079..6814818hg19UCSC Ensembl
Cytoband1p36.31
Allele length
AssemblyAllele length
hg382740
hg192740
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18204316
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326950
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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