A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1112229



Internal ID19278751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5159883..5282783hg38UCSC Ensembl
Outerchr10:5202082..5324746hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38122901
hg19122665
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv350n106
Supporting Variantsnssv3965926
SamplesKWS2
Known GenesAKR1C4, AKR1CL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1112229
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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