A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17414238



Internal ID22472108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:162740036..162740196hg38UCSC Ensembl
chr4:163661188..163661348hg19UCSC Ensembl
Cytoband4q32.2
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5901436
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17414238
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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