A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320070



Internal ID20853168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:100994740..101002064hg38UCSC Ensembl
chr1:101460296..101467620hg19UCSC Ensembl
Cytoband1p21.2
Allele length
AssemblyAllele length
hg387325
hg197325
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18049641
Samples
Known GenesDPH5
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320070
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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