A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16267762



Internal ID20476980
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:55909926..55909981hg38UCSC Ensembl
chr6:55774724..55774779hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4745338
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16267762
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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