A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110068



Internal ID19271261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:134792840..134792910hg38UCSC Ensembl
Outerchr9:137684686..137684756hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv4162n106
Supporting Variantsnssv3959306
SamplesKWS1
Known GenesCOL5A1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110068
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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