A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3952853



Internal ID21372923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131785029..131785145hg38UCSC Ensembl
chr5:131120722..131120838hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38117
hg19117
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15197535
SamplesHG002
Known GenesFNIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3952853
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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