A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5529913



Internal ID305913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82324787..82338930hg38UCSC Ensembl
chr15:82617143..82631284hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3814144
hg1914142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17704060
Samples
Known GenesADAMTS7P1
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5529913
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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