A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135934



Internal ID18902691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:9955229..9955514hg38UCSC Ensembl
Outerchr4:9956853..9957138hg19UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg38286
hg19286
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2736n106
Supporting Variantsnssv3989531
SamplesKWS2
Known GenesSLC2A9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135934
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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