A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1124331



Internal ID18916893
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:27660611..27660686hg38UCSC Ensembl
Outerchr8:27518128..27518203hg19UCSC Ensembl
Cytoband8p21.1
Allele length
AssemblyAllele length
hg3876
hg1976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3798n106
Supporting Variantsnssv3975632
SamplesKWS2
Known GenesSCARA3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1124331
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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