A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980875



Internal ID18876185
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:17389153..17389653hg38UCSC Ensembl
Outerchr11:17410700..17411200hg19UCSC Ensembl
Cytoband11p15.1
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118206
Supporting Variants
SamplesKWS1
Known GenesKCNJ11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980875
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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