A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17423897



Internal ID22481767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:6658062..6658196hg38UCSC Ensembl
chr5:6658175..6658309hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg38135
hg19135
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5893824
Supporting Variants
Samples
Known GenesSRD5A1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17423897
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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