A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333571



Internal ID20866750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16103201..16107400hg38UCSC Ensembl
chr1:16429696..16433895hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv97n223
Supporting Variantsnssv18052491
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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