A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5951635



Internal ID22726994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:185290720..185290720hg38UCSC Ensembl
chr4:186211874..186211874hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17413916
Samples
Known GenesSNX25
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5951635
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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