A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17579872



Internal ID21771915
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:55120513..55120513hg38UCSC Ensembl
chr8:56033073..56033073hg19UCSC Ensembl
Cytoband8q12.1
Allele length
AssemblyAllele length
hg38320
hg19320
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6061991
Supporting Variants
Samples
Known GenesXKR4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17579872
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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