A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1149325



Internal ID19196080
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5159893..5282757hg38UCSC Ensembl
Outerchr10:5202092..5324720hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38122865
hg19122629
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4002835
SamplesKWB1
Known GenesAKR1C4, AKR1CL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nsv1149325
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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