A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6512953



Internal ID20886293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:98825021..98827679hg38UCSC Ensembl
chr15:99368250..99370908hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382659
hg192659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027648
Samples
Known GenesIGF1R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6512953
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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