A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17564837



Internal ID21889192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:8526570..8553866hg38UCSC Ensembl
chr6:8526803..8554099hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3827297
hg1927297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6007481
Supporting Variants
Samples
Known GenesLOC100506207
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17564837
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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