A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331438



Internal ID20864601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:2263529..2285169hg38UCSC Ensembl
chr1:2194968..2216608hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3821641
hg1921641
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058413
Samples
Known GenesSKI
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331438
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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