A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608582



Internal ID20981653
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:41852789..41882889hg38UCSC Ensembl
chr7:41892387..41922487hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3830101
hg1930101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18231454
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608582
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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