A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009644



Internal ID21918987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76339423..76340040hg38UCSC Ensembl
chr7:75968740..75969357hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38618
hg19618
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576064
Samples
Known GenesYWHAG
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009644
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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