A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615938



Internal ID20989009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:119393201..119437700hg38UCSC Ensembl
chr7:119033255..119077754hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3844500
hg1944500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7096n223
Supporting Variantsnssv18229962
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615938
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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