A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1137666



Internal ID19253303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:100427118..100427418hg38UCSC Ensembl
Outerchr9:103189400..103189700hg19UCSC Ensembl
Cytoband9q31.1
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4107n106
Supporting Variantsnssv3990168
SamplesKWS2
Known GenesMSANTD3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1137666
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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