A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6614613



Internal ID20987684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1856061..2154141hg38UCSC Ensembl
chr7:1895697..2193776hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38298081
hg19298080
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18227961
Samples
Known GenesMAD1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6614613
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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