A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6332027



Internal ID20865196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:23626648..23628258hg38UCSC Ensembl
chr1:23953138..23954748hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg381611
hg191611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058922
Samples
Known GenesMDS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6332027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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