A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6513705



Internal ID20887052
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:57658564..57659014hg38UCSC Ensembl
chr15:57950762..57951212hg19UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg38451
hg19451
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18025295
Samples
Known GenesGCOM1, MYZAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6513705
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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