A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17135195



Internal ID21497695
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:143031405..143031405hg38UCSC Ensembl
chr3:142750247..142750247hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg3888
hg1988
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5619705
Supporting Variants
SamplesNA19238
Known GenesU2SURP
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nssv17135195
Frequency
Sample Size35
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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