A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011831



Internal ID21921174
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36243724..36244062hg38UCSC Ensembl
chr7:36283333..36283671hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg38339
hg19339
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559196
Samples
Known GenesEEPD1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011831
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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