A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606396



Internal ID20979467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107794034..107807824hg38UCSC Ensembl
chr7:107434479..107448269hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3813791
hg1913791
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236080
Samples
Known GenesSLC26A3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606396
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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