A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958027



Internal ID16960214
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68397160..68397284hg38UCSC Ensembl
Outerchr15:68689499..68689623hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3005559
SamplesBILGI_BIOE
Known GenesITGA11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958027
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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