A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608510



Internal ID20981581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:2119597..2214746hg38UCSC Ensembl
chr7:2159232..2254381hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3895150
hg1995150
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156941
Samples
Known GenesMAD1L1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608510
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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