A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747831



Internal ID20523852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:75712127..75712290hg38UCSC Ensembl
chr2:75939253..75939416hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284643
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747831
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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