A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952175



Internal ID16954362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:49323118..49346117hg38UCSC Ensembl
Outerchr12:49716901..49739900hg19UCSC Ensembl
Cytoband12q13.12
Allele length
AssemblyAllele length
hg3823000
hg1923000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999725
SamplesBILGI_BIOE
Known GenesC1QL4, TROAP
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952175
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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