A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1126876



Internal ID19273650
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:60937707..60960617hg38UCSC Ensembl
Outerchr9:39908200..39931100hg19UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg3822911
hg1922901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3985153
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1126876
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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