A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320925



Internal ID20854026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100485475..100488737hg38UCSC Ensembl
chr1:100951031..100954293hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg383263
hg193263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049593
Samples
Known GenesCDC14A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320925
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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