A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110540



Internal ID19263461
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:61062171..61080648hg38UCSC Ensembl
Outerchr9:43877400..43895900hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg3818478
hg1918501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960193
SamplesKWS1
Known GenesCNTNAP3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110540
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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