A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6498747



Internal ID20871960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84619366..84624287hg38UCSC Ensembl
chr15:85162597..85167518hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg384922
hg194922
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18027228
Samples
Known GenesZSCAN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6498747
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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