A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002663



Internal ID16948929
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:74301861..74302051hg38UCSC Ensembl
Outerchr17:72298000..72298190hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg38191
hg19191
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954601
Supporting Variants
SamplesBILGI_BIOE
Known GenesDNAI2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002663
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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