A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6507123



Internal ID20880411
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:92751042..93010689hg38UCSC Ensembl
chr15:93294272..93553919hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg38259648
hg19259648
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18190420
Samples
Known GenesASB9P1, CHD2, LOC100507217, MIR3175
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6507123
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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