A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4736876



Internal ID20512829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:76723098..76741732hg38UCSC Ensembl
chr1:77188783..77207417hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3818635
hg1918635
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4736876
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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