A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16295287



Internal ID20504505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196614476..196614570hg38UCSC Ensembl
chr3:196341347..196341441hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743373
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16295287
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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