A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17493535



Internal ID22551464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:155839595..155845790hg38UCSC Ensembl
chr4:156760747..156766942hg19UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg386196
hg196196
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5837767
Supporting Variants
Samples
Known GenesASIC5
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17493535
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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