A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600335



Internal ID20973406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:117077844..117080061hg38UCSC Ensembl
chr7:116717898..116720115hg19UCSC Ensembl
Cytoband7q31.2
Allele length
AssemblyAllele length
hg382218
hg192218
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229901
Samples
Known GenesST7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600335
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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