A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998827



Internal ID16945093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:82297625..82408424hg38UCSC Ensembl
Outerchr17:80255501..80366300hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38110800
hg19110800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952394
Supporting Variants
SamplesBILGI_BIOE
Known GenesCD7, OGFOD3, SECTM1, TEX19, UTS2R
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998827
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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