A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011463



Internal ID21920806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123735456..123735517hg38UCSC Ensembl
chr7:123375510..123375571hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17570800
Samples
Known GenesWASL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011463
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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