A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616125



Internal ID20989196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:15670776..15672968hg38UCSC Ensembl
chr7:15710401..15712593hg19UCSC Ensembl
Cytoband7p21.2
Allele length
AssemblyAllele length
hg382193
hg192193
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151467
Samples
Known GenesMEOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616125
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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