A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023595



Internal ID21932938
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:56710735..56712121hg38UCSC Ensembl
chr12:57104519..57105905hg19UCSC Ensembl
Cytoband12q13.3
Allele length
AssemblyAllele length
hg381387
hg191387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17598566
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023595
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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