A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6586672



Internal ID20959743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:88103257..88110133hg38UCSC Ensembl
chr15:88646488..88653364hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg386877
hg196877
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18240525
Samples
Known GenesNTRK3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6586672
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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