A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997532



Internal ID19194737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:117256078..117271368hg38UCSC Ensembl
Outerchr10:119015589..119030879hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg3815291
hg1915291
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1148753
Supporting Variants
SamplesKWB1
Known GenesSLC18A2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997532
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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