A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6605214



Internal ID20978285
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101291401..102143126hg38UCSC Ensembl
chr7:100934682..101786406hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38851726
hg19851725
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18234664
Samples
Known GenesCOL26A1, CUX1, LINC01007, MYL10, RABL5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6605214
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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