A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1119276



Internal ID19252225
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:61094251..61102388hg38UCSC Ensembl
Outerchr9:43855700..43863800hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg388138
hg198101
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3959713
SamplesKWS1
Known GenesCNTNAP3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1119276
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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