A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3950667



Internal ID21370736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:154744623..154744938hg38UCSC Ensembl
chr5:154124183..154124498hg19UCSC Ensembl
Cytoband5q33.2
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15196767
SamplesHG002
Known GenesLARP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3950667
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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