A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122362



Internal ID19270380
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136302171..136307357hg38UCSC Ensembl
Outerchr3:136021013..136026199hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg385187
hg195187
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2607n106
Supporting Variantsnssv3970569
SamplesKWS1
Known GenesPCCB
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122362
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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