A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17565117



Internal ID21889472
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178900407..178900407hg38UCSC Ensembl
chr5:178327408..178327408hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6063422
Supporting Variants
Samples
Known GenesZFP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17565117
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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