A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997381



Internal ID17290333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:130331156..130340955hg38UCSC Ensembl
Outerchr12:130815701..130825500hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg389800
hg199800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952507
Supporting Variants
SamplesBILGI_BIOE
Known GenesPIWIL1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997381
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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