A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16276778



Internal ID20485996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:35136441..35137044hg38UCSC Ensembl
chr6:35104218..35104821hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38604
hg19604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4738122
Supporting Variants
Samples
Known GenesTCP11
MethodSequencing
Analysis
Platform
Comments
ReferenceQuan_et_al_2021
Pubmed ID34034800
Accession Number(s)nssv16276778
Frequency
Sample Size25
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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