A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6613602



Internal ID20986673
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 StatusM
Merged Variants
Supporting Variantsnssv18155453
Samples
Known GenesAP5Z1, MIR4656, PAPOLB, RADIL
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6613602
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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