A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1132887



Internal ID19255835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:29622557..29622611hg38UCSC Ensembl
Outerchr19:30113464..30113518hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3987681
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1132887
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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