A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424002



Internal ID21081555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140206168..140291586hg38UCSC Ensembl
chr7:139905968..139991386hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3885419
hg1985419
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236766
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424002
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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