A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3004201



Internal ID17297153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:14792458..14792549hg38UCSC Ensembl
Outerchr12:14945392..14945483hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3892
hg1992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957913
Supporting Variants
SamplesBILGI_BIOE
Known GenesWBP11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3004201
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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