A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615428



Internal ID20988499
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:105562532..105583090hg38UCSC Ensembl
chr7:105202979..105223537hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3820559
hg1920559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152065
Samples
Known GenesEFCAB10, RINT1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615428
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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