A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325032



Internal ID20858162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17310780..17310917hg38UCSC Ensembl
chr1:17637275..17637412hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38138
hg19138
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053969
Samples
Known GenesPADI4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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