A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17413160



Internal ID22471030
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:122357887..122358767hg38UCSC Ensembl
chr5:121693582..121694462hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg38881
hg19881
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893016
Supporting Variants
Samples
Known GenesSNCAIP
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17413160
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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