A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137554



Internal ID19263810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:111871597..111875397hg38UCSC Ensembl
Outerchr6:112192800..112196600hg19UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg383801
hg193801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990058
SamplesKWS2
Known GenesFYN
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137554
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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