A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1111823



Internal ID19263322
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:17376369..17381169hg38UCSC Ensembl
Outerchr6:17376600..17381400hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg384801
hg194801
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3277n106
Supporting Variantsnssv3964732
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1111823
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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