A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4762604



Internal ID20538464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:80113816..80113816hg38UCSC Ensembl
chr17:78087615..78087615hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38306
hg19306
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16288241
Samples
Known GenesGAA
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4762604
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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