A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1144713



Internal ID19251523
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:29535758..29535823hg38UCSC Ensembl
Outerchr14:30004964..30005029hg19UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3995598
SamplesKWS1
Known GenesMIR548AI
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1144713
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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