A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009552



Internal ID21918895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:96996019..96996104hg38UCSC Ensembl
chr7:96625331..96625416hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3886
hg1986
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572278
Samples
Known GenesDLX6-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009552
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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