A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507138



Internal ID20880426
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:83946140..83946419hg38UCSC Ensembl
chr15:84614892..84615171hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38280
hg19280
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027214
Samples
Known GenesADAMTSL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507138
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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