A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16275139



Internal ID20484357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139769289..139769289hg38UCSC Ensembl
chr7:139469088..139469088hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3859
hg1959
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4762088
Supporting Variants
Samples
Known GenesHIPK2
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16275139
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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