A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970485



Internal ID18886987
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:63854365..63854440hg38UCSC Ensembl
Outerchr11:63621837..63621912hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1134138
Supporting Variants
SamplesKWS2
Known GenesMARK2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970485
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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