A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17427572



Internal ID22485442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:74777989..74778069hg38UCSC Ensembl
chr4:75703199..75703279hg19UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5898851
Supporting Variants
Samples
Known GenesBTC
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17427572
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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