A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6001147



Internal ID21910490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50459880..50459941hg38UCSC Ensembl
chr7:50527578..50527639hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17558872
Samples
Known GenesDDC
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6001147
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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