A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493705



Internal ID22551634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:186176909..186194470hg38UCSC Ensembl
chr4:187098063..187115624hg19UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3817562
hg1917562
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839080
Supporting Variants
Samples
Known GenesCYP4V2, FLJ38576
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493705
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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