A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003974



Internal ID19188571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:43368284..43368572hg38UCSC Ensembl
Outerchr15:43660482..43660770hg19UCSC Ensembl
Cytoband15q15.3
Allele length
AssemblyAllele length
hg38289
hg19289
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151412
Supporting Variants
SamplesKWB1
Known GenesZSCAN29
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003974
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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