A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332705



Internal ID20865879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:104006997..104108319hg38UCSC Ensembl
chr1:104549619..104650941hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg38101323
hg19101323
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18200342
Samples
Known GenesLOC100129138
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332705
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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