A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3994487



Internal ID18856866
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:99566095..99566595hg38UCSC Ensembl
Outerchr15:100106300..100106800hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1143792
Supporting Variants
SamplesKWS1
Known GenesMEF2A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3994487
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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