A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958682



Internal ID17307555
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:64366481..64366750hg38UCSC Ensembl
Outerchr12:64760261..64760530hg19UCSC Ensembl
Cytoband12q14.2
Allele length
AssemblyAllele length
hg38270
hg19270
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004115
SamplesBILGI_BIOE
Known GenesC12orf56
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958682
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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