A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137125



Internal ID18924362
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:89981071..89981134hg38UCSC Ensembl
Outerchr6:90690790..90690853hg19UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3975814
SamplesKWS2
Known GenesBACH2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137125
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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