A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6000764



Internal ID21910107
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121923413..121923491hg38UCSC Ensembl
chr7:121563467..121563545hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17557695
Samples
Known GenesPTPRZ1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6000764
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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