A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998739



Internal ID16945005
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:38527166..38590447hg38UCSC Ensembl
Outerchr17:36683401..36746700hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3863282
hg1963300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953893
Supporting Variants
SamplesBILGI_BIOE
Known GenesSRCIN1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998739
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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