A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119080



Internal ID18936772
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:35496523..35497423hg38UCSC Ensembl
Outerchr6:35464300..35465200hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3299n106
Supporting Variantsnssv3981880
SamplesKWS1
Known GenesTEAD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119080
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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