A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001569



Internal ID17294521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:63863130..63901457hg38UCSC Ensembl
Outerchr17:61940490..61978817hg19UCSC Ensembl
Cytoband17q23.3
Allele length
AssemblyAllele length
hg3838328
hg1938328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv954553
Supporting Variants
SamplesBILGI_BIOE
Known GenesCSH1, CSH2, GH2, TCAM1P
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001569
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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