A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133749



Internal ID19251688
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:136033454..136056554hg38UCSC Ensembl
Outerchr9:138925300..138948400hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3823101
hg1923101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4169n106
Supporting Variantsnssv3969324
SamplesKWS2
Known GenesNACC2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133749
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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