A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1127298



Internal ID18937757
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:121163580..121163633hg38UCSC Ensembl
Outerchr12:121601383..121601436hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985705
SamplesKWS1
Known GenesP2RX7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1127298
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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