A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1145265



Internal ID19262184
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:127568821..127569221hg38UCSC Ensembl
Outerchr9:130331100..130331500hg19UCSC Ensembl
Cytoband9q34.11
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3982352
SamplesKWS1
Known GenesFAM129B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1145265
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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