A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4001939



Internal ID18844131
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:23549736..23550347hg38UCSC Ensembl
Outerchr8:23407249..23407860hg19UCSC Ensembl
Cytoband8p21.2
Allele length
AssemblyAllele length
hg38612
hg19612
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1151006
Supporting Variants
SamplesKWB1
Known GenesSLC25A37
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4001939
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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