A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4767195



Internal ID20543055
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:60349820..60349820hg38UCSC Ensembl
chr15:60642019..60642019hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg38534
hg19534
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16284205
Samples
Known GenesANXA2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4767195
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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