A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6499780



Internal ID20873004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:67945905..67946411hg38UCSC Ensembl
chr15:68238243..68238749hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38507
hg19507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025484
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6499780
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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