A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136278



Internal ID18910476
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:10960724..10962024hg38UCSC Ensembl
Outerchr19:11071400..11072700hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg381301
hg191301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989895
SamplesKWS2
Known GenesSMARCA4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136278
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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