A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258976



Internal ID20468164
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155846942..155846942hg38UCSC Ensembl
chr7:155639636..155639636hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38172
hg19172
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4767217
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16258976
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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