A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126265



Internal ID18923664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:67731252..67731532hg38UCSC Ensembl
Outerchr17:65727368..65727648hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg38281
hg19281
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1499n106
Supporting Variantsnssv3984498
SamplesKWS1
Known GenesNOL11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126265
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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