A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109270



Internal ID18931793
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:29423248..29423783hg38UCSC Ensembl
Outerchr10:29712177..29712712hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38536
hg19536
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv387n106
Supporting Variantsnssv3955919
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109270
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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