A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126188



Internal ID18921650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:93822800..93825708hg38UCSC Ensembl
Outerchr1:94288356..94291264hg19UCSC Ensembl
Cytoband1p22.1
Allele length
AssemblyAllele length
hg382909
hg192909
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv127n106
Supporting Variantsnssv3984417
SamplesKWS1
Known GenesBCAR3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126188
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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