A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951026



Internal ID16953213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:67994030..68053133hg38UCSC Ensembl
Outerchr11:67761501..67820600hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg3859104
hg1959100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999574
SamplesBILGI_BIOE
Known GenesALDH3B1, CHKA, MIR4691, MIR6753, MIR7113, NDUFS8, TCIRG1, UNC93B1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951026
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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