A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955421



Internal ID16957608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:39498940..39499207hg38UCSC Ensembl
Outerchr17:37655193..37655460hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38268
hg19268
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001536
SamplesBILGI_BIOE
Known GenesCDK12
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955421
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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