A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004004



Internal ID21913347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:14249392..14283150hg38UCSC Ensembl
chr7:14289017..14322775hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3833759
hg1933759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566445
Samples
Known GenesDGKB
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004004
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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