A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316159



Internal ID20849237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15617201..15617700hg38UCSC Ensembl
chr1:15943696..15944195hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg38500
hg19500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052253
Samples
Known GenesDDI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316159
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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