A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998148



Internal ID17291100
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:8701054..8735653hg38UCSC Ensembl
Outerchr11:8722601..8757200hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg3834600
hg1934600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951306
Supporting Variants
SamplesBILGI_BIOE
Known GenesST5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998148
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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