A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329957



Internal ID20863111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:116756039..116765564hg38UCSC Ensembl
chr1:117298661..117308186hg19UCSC Ensembl
Cytoband1p13.1
Allele length
AssemblyAllele length
hg389526
hg199526
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18199753
Samples
Known GenesCD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329957
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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