A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16285078



Internal ID20494296
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:66735526..66735853hg38UCSC Ensembl
chr1:67201209..67201536hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4743189
Supporting Variants
Samples
Known GenesSGIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16285078
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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