A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325550



Internal ID20858681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106319951..106382564hg38UCSC Ensembl
chr1:106862573..106925186hg19UCSC Ensembl
Cytoband1p21.1
Allele length
AssemblyAllele length
hg3862614
hg1962614
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050718
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325550
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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