A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4732962



Internal ID20508888
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:241105152..241105208hg38UCSC Ensembl
chr1:241268452..241268508hg19UCSC Ensembl
Cytoband1q43
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16281456
Samples
Known GenesRGS7
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4732962
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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