A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610015



Internal ID20983086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:90593101..90601200hg38UCSC Ensembl
chr7:90222415..90230514hg19UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg388100
hg198100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18233713
Samples
Known GenesCDK14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610015
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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