A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6014263



Internal ID21923606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:44768559..44770992hg38UCSC Ensembl
chr7:44808158..44810591hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg382434
hg192434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17566165
Samples
Known GenesZMIZ2
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6014263
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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