A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138216



Internal ID19249112
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:37439661..37439732hg38UCSC Ensembl
Outerchr13:38013798..38013869hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983334, nssv3971787
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138216
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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