A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4735242



Internal ID20511184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:127596025..127596093hg38UCSC Ensembl
chr9:130358304..130358372hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg3869
hg1969
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16285650
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4735242
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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