A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3993180



Internal ID18867988
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:95302056..96435607hg38UCSC Ensembl
Outerchr15:95845285..96978837hg19UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg381133552
hg191133553
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1141674
Supporting Variants
SamplesKWS1
Known GenesLINC00924, LOC400456, MIR1469, NR2F2, NR2F2-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3993180
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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