A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133471



Internal ID19261521
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:61536565..61538265hg38UCSC Ensembl
Outerchr2:61763700..61765400hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg381701
hg191701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969032
SamplesKWS2
Known GenesXPO1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133471
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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