A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127173



Internal ID19265109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:33345546..33345618hg38UCSC Ensembl
Outerchr11:33367092..33367164hg19UCSC Ensembl
Cytoband11p13
Allele length
AssemblyAllele length
hg3873
hg1973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985544
SamplesKWS1
Known GenesHIPK3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127173
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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