A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3964126



Internal ID19203759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:102601126..102601432hg38UCSC Ensembl
Outerchr11:102471857..102472163hg19UCSC Ensembl
Cytoband11q22.2
Allele length
AssemblyAllele length
hg38307
hg19307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120917
Supporting Variants
SamplesKWS1
Known GenesMMP20
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3964126
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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