A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615082



Internal ID20988153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87839101..87841100hg38UCSC Ensembl
chr7:87468416..87470415hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18161877
Samples
Known GenesSLC25A40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615082
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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