A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4740962



Internal ID20516939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:112706424..112706488hg38UCSC Ensembl
chr1:113249046..113249110hg19UCSC Ensembl
Cytoband1p13.2
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284849
Samples
Known GenesRHOC
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4740962
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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