A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6466501



Internal ID21124054
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29408001..29408400hg38UCSC Ensembl
chr12:29560934..29561333hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38400
hg19400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17998588
Samples
Known GenesOVCH1-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6466501
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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