A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5600853



Internal ID21549496
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29420474..29420814hg38UCSC Ensembl
chr12:29573407..29573747hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38341
hg19341
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17079377
SamplesHG00731
Known GenesOVCH1-AS1
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5600853
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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