A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333392



Internal ID20866568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:72477796..72478156hg38UCSC Ensembl
chr1:72943479..72943839hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38361
hg19361
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333392
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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