A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155453



Internal ID20722493
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:4785714..4879579hg38UCSC Ensembl
chr7:4825345..4919210hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3893866
hg1993866
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6613602
Supporting Variants
Samples
Known GenesAP5Z1, MIR4656, PAPOLB, RADIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155453
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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