A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135910



Internal ID21497601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:196334808..196335018hg38UCSC Ensembl
chr3:196061679..196061889hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5575676
Supporting Variants
SamplesNA19238
Known GenesTM4SF19, TM4SF19-TCTEX1D2
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135910
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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