A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124064



Internal ID19264613
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:54915508..54915836hg38UCSC Ensembl
Outerchr6:54780306..54780634hg19UCSC Ensembl
Cytoband6p12.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974245
SamplesKWS2
Known GenesFAM83B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124064
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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