A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126181



Internal ID18907217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:15523805..15525705hg38UCSC Ensembl
Outerchr1:15850300..15852200hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3984410
SamplesKWS1
Known GenesCASP9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126181
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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