A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3005528



Internal ID16951794
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68421006..68421209hg38UCSC Ensembl
Outerchr15:68713345..68713548hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg38204
hg19204
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv957995
Supporting Variants
SamplesBILGI_BIOE
Known GenesITGA11
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3005528
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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