A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008630



Internal ID21917973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44557604..44557697hg38UCSC Ensembl
chr7:44597203..44597296hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3894
hg1994
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17575216
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008630
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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