A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17570710



Internal ID21762753
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:160474386..160474471hg38UCSC Ensembl
chr5:159901393..159901478hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6005710
Supporting Variants
Samples
Known GenesMIR3142
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17570710
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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