A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009432



Internal ID21918775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55402331..55402453hg38UCSC Ensembl
chr7:55470024..55470146hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17565462
Samples
Known GenesLANCL2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009432
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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