A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3985590



Internal ID19215011
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:72562941..72563002hg38UCSC Ensembl
Outerchr11:72273985..72274046hg19UCSC Ensembl
Cytoband11q13.4
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127208
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3985590
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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