A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011538



Internal ID21920881
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156539621..156539757hg38UCSC Ensembl
chr7:156332315..156332451hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38137
hg19137
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564687
Samples
Known GenesLINC01006
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011538
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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