A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608040



Internal ID20981111
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37112245..37118031hg38UCSC Ensembl
chr7:37151850..37157636hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg385787
hg195787
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156204
Samples
Known GenesELMO1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608040
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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