A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617833



Internal ID20990904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74137154..74141318hg38UCSC Ensembl
chr7:73551484..73555648hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384165
hg194165
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221658
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617833
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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