A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15751681



Internal ID21388440
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:44340604..44345351hg38UCSC Ensembl
chr3:44382096..44386843hg19UCSC Ensembl
Cytoband3p21.31
Allele length
AssemblyAllele length
hg384748
hg194748
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4434059
Supporting Variants
SamplesNB07
Known GenesTCAIM
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15751681
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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