A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616099



Internal ID20989170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108060286..108121665hg38UCSC Ensembl
chr7:107700731..107762110hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3861380
hg1961380
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221164
Samples
Known GenesLAMB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616099
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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