A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129395



Internal ID19258674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:61362511..61362609hg38UCSC Ensembl
Outerchr2:61589646..61589744hg19UCSC Ensembl
Cytoband2p15
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962834
SamplesKWS1
Known GenesUSP34
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129395
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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