A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999637



Internal ID16945903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:125070905..125093704hg38UCSC Ensembl
Outerchr11:124940801..124963600hg19UCSC Ensembl
Cytoband11q24.2
Allele length
AssemblyAllele length
hg3822800
hg1922800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952754
Supporting Variants
SamplesBILGI_BIOE
Known GenesSLC37A2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999637
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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