A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606594



Internal ID20979665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:113529401..113539700hg38UCSC Ensembl
chr7:113169456..113179755hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3810300
hg1910300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7088n223
Supporting Variantsnssv18231618
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606594
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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