A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6322673



Internal ID20855786
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:94541001..94542800hg38UCSC Ensembl
chr1:95006557..95008356hg19UCSC Ensembl
Cytoband1p21.3
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18203194
Samples
Known GenesF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6322673
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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