A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014277



Internal ID21923620
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:178900466..178900561hg38UCSC Ensembl
chr5:178327467..178327562hg19UCSC Ensembl
Cytoband5q35.3
Allele length
AssemblyAllele length
hg3896
hg1996
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17560987
Samples
Known GenesZFP2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014277
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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