A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1133741



Internal ID19256072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:127568421..127569321hg38UCSC Ensembl
Outerchr9:130330700..130331600hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969315
SamplesKWS2
Known GenesFAM129B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1133741
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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