A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137671



Internal ID18931421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:129664921..129667521hg38UCSC Ensembl
Outerchr9:132427200..132429800hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg382601
hg192601
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3990172
SamplesKWS2
Known GenesPRRX2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137671
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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