A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005397



Internal ID20572437
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 StatusS
Merged Variantsnsv6470449
Supporting Variants
Samples
Known GenesCCDC41
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005397
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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