A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17576811



Internal ID21768854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138945173..138946032hg38UCSC Ensembl
chr7:138629919..138630778hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg38860
hg19860
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6019263
Supporting Variants
Samples
Known GenesKIAA1549
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17576811
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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