A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968679



Internal ID19235866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:62212110..62212175hg38UCSC Ensembl
Outerchr11:61979582..61979647hg19UCSC Ensembl
Cytoband11q12.3
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1113397
Supporting Variants
SamplesKWS2
Known GenesSCGB2A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968679
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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