A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495918



Internal ID22553851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:53204195..53218918hg38UCSC Ensembl
chr4:54070362..54085085hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3814724
hg1914724
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839070
Supporting Variants
Samples
Known GenesSCFD2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495918
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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