A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6611337



Internal ID20984408
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:57734939..57976360hg38UCSC Ensembl
chr7:57794645..58036066hg19UCSC Ensembl
Cytoband7p11.1
Allele length
AssemblyAllele length
hg38241422
hg19241422
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6689n223
Supporting Variantsnssv18223585
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6611337
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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