A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011795



Internal ID21921138
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:68509835..68509886hg38UCSC Ensembl
chr7:67974822..67974873hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17564955
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011795
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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