A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3991076



Internal ID18893166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9227575..9227626hg38UCSC Ensembl
Outerchr17:9130892..9130943hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1138499
Supporting Variants
SamplesKWS2
Known GenesNTN1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3991076
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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