A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610601



Internal ID20983672
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15600701..15621900hg38UCSC Ensembl
chr7:15640326..15661525hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg3821200
hg1921200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220619
Samples
Known GenesMEOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610601
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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