A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16272804



Internal ID20482022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16132148..16134448hg38UCSC Ensembl
chr7:16171773..16174073hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg382301
hg192301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4744710
Supporting Variants
Samples
Known GenesISPD
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16272804
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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