A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610311



Internal ID20983382
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101526138..101698760hg38UCSC Ensembl
chr7:101169419..101342040hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38172623
hg19172622
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18225667
Samples
Known GenesCOL26A1, LINC01007, MYL10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610311
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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