A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111641



Internal ID19278319
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:58562832..58569367hg38UCSC Ensembl
Outerchr4:59428997..59435532hg19UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg386536
hg196536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2804n106
Supporting Variantsnssv3964537
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111641
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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