A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352907



Internal ID21010460
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68045501..68047000hg38UCSC Ensembl
chr2:68272633..68274132hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg381500
hg191500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088815
Samples
Known GenesC1D
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352907
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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