A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4747520



Internal ID20523538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:6154138..6154363hg38UCSC Ensembl
chr17:6057458..6057683hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg38226
hg19226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16290521
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nsv4747520
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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