A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321872



Internal ID20854980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:143535201..143622600hg38UCSC Ensembl
chr1:149029863..149117261hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3887400
hg1987399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv333n223
Supporting Variantsnssv18200730
Samples
Known GenesLOC101929780
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321872
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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