A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1130199



Internal ID19266860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:5763270..5788070hg38UCSC Ensembl
Outerchr11:5784500..5809300hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3824801
hg1924801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv580n106
Supporting Variantsnssv3964197, nssv3960437
SamplesKWS2, KWS1
Known GenesOR52N1, OR52N5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1130199
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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