A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv958125



Internal ID17306998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr13:36840274..36840652hg38UCSC Ensembl
Outerchr13:37414411..37414789hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg38379
hg19379
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3004283
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv958125
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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