A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332632



Internal ID20865805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:47498601..47500300hg38UCSC Ensembl
chr1:47964273..47965972hg19UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061611
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332632
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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