A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3955114



Internal ID19218498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:27365226..27365320hg38UCSC Ensembl
Outerchr15:27610372..27610466hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3895
hg1995
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1127419
Supporting Variants
SamplesKWS1
Known GenesGABRG3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3955114
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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