A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6470449



Internal ID21128002
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:94314801..94316500hg38UCSC Ensembl
chr12:94708577..94710276hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381700
hg191700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18005397
Samples
Known GenesCCDC41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6470449
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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