A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981000



Internal ID18862240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74782059..74782659hg38UCSC Ensembl
Outerchr15:75074400..75075000hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg38601
hg19601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118322
Supporting Variants
SamplesKWS1
Known GenesCSK
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981000
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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