A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3992442



Internal ID19220127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:5159903..5282762hg38UCSC Ensembl
Outerchr10:5202102..5324725hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg38122860
hg19122624
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140934
Supporting Variants
SamplesKWS1
Known GenesAKR1C4, AKR1CL1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3992442
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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