A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17557247



Internal ID21881602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:43578235..43578286hg38UCSC Ensembl
chr5:43578337..43578388hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6000132
Supporting Variants
Samples
Known GenesNNT-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17557247
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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