A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001539



Internal ID17294491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:15960311..15960576hg38UCSC Ensembl
Outerchr17:15863625..15863890hg19UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955424
Supporting Variants
SamplesBILGI_BIOE
Known GenesADORA2B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001539
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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