A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17573877



Internal ID21765920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178907569..178912144hg38UCSC Ensembl
chr5:178334570..178339145hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg384576
hg194576
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6017673
Supporting Variants
Samples
Known GenesZFP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17573877
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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