A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17587398



Internal ID21779441
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:1584693..1584693hg38UCSC Ensembl
chr11:1605923..1605923hg19UCSC Ensembl
Cytoband11p15.5
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6086802
Supporting Variants
Samples
Known GenesKRTAP5-1, KRTAP5-AS1, MOB2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17587398
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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