A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6497598



Internal ID20870806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:91206075..91207154hg38UCSC Ensembl
chr15:91749305..91750384hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg381080
hg191080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027410
Samples
Known GenesSV2B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6497598
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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