A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610559



Internal ID20983630
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:42909301..42914600hg38UCSC Ensembl
chr7:42948900..42954199hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg385300
hg195300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18221031
Samples
Known GenesC7orf25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610559
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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