A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3000215



Internal ID17293167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:1064861..1162806hg38UCSC Ensembl
Outerchr17:968101..1066100hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg3897946
hg1998000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952096
Supporting Variants
SamplesBILGI_BIOE
Known GenesABR
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3000215
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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