A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6147381



Internal ID346562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:78765911..78766103hg38UCSC Ensembl
chr15:79058253..79058445hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg38193
hg19193
Variant TypeOTHER sequence alteration
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17702209
Samples
Known GenesADAMTS7
MethodSequencing
Analysis
Platform
Commentscomplex variant
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6147381
Frequency
Sample Size3202
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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