A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126325



Internal ID18901213
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:11826278..11826399hg38UCSC Ensembl
Outerchr18:11826277..11826398hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38122
hg19122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1552n106
Supporting Variantsnssv3984564
SamplesKWS1
Known GenesGNAL
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126325
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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