A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16277046



Internal ID20486264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155973756..155973756hg38UCSC Ensembl
chr7:155766450..155766450hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4756325
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16277046
Frequency
Sample Size25
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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