A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5953177



Internal ID22728471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53578919..53578919hg38UCSC Ensembl
chr4:54445086..54445086hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg38283
hg19283
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17415802
Samples
Known GenesLNX1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5953177
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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