A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6472337



Internal ID21129890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:28312723..28313342hg38UCSC Ensembl
chr12:28465656..28466275hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38620
hg19620
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18000154
Samples
Known GenesCCDC91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6472337
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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