A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4757609



Internal ID20533469
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:17030459..17030459hg38UCSC Ensembl
chr17:16933773..16933773hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38305
hg19305
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16273625
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4757609
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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