A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114386



Internal ID19280702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:64310459..64310522hg38UCSC Ensembl
Outerchr3:64296135..64296198hg19UCSC Ensembl
Cytoband3p14.1
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3956600, nssv3973903
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114386
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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