A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615185



Internal ID20988256
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:125190020..125190308hg38UCSC Ensembl
chr7:124830074..124830362hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150860
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615185
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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