A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960193



Internal ID19216526
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 StatusS
Merged Variantsnsv1110540
Supporting Variants
SamplesKWS1
Known GenesCNTNAP3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960193
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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