A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513606



Internal ID20886952
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:80838108..80840213hg38UCSC Ensembl
chr15:81130449..81132554hg19UCSC Ensembl
Cytoband15q25.1
Allele length
AssemblyAllele length
hg382106
hg192106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026439
Samples
Known GenesKIAA1199
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513606
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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