A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17495138



Internal ID22553071
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:4412205..4414468hg38UCSC Ensembl
chr4:4413932..4416195hg19UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg382264
hg192264
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5839030
Supporting Variants
Samples
Known GenesNSG1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17495138
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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