A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000295



Internal ID16946561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:29618383..29623782hg38UCSC Ensembl
Outerchr17:27945401..27950800hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953874
Supporting Variants
SamplesBILGI_BIOE
Known GenesCORO6
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000295
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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