A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4758663



Internal ID20534523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:5812574..5812574hg38UCSC Ensembl
chr12:5921740..5921740hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38162
hg19162
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16295572
Samples
Known GenesANO2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4758663
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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