A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3984644



Internal ID18874780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:68817861..68825761hg38UCSC Ensembl
Outerchr15:69110200..69118100hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387901
hg197901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1126398
Supporting Variants
SamplesKWS1
Known GenesANP32A, MIR548H4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3984644
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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