A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1118829



Internal ID19263353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:39320660..39321060hg38UCSC Ensembl
Outerchr19:39811300..39811700hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1781n106
Supporting Variantsnssv3981144
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1118829
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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