A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3961681



Internal ID19205799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:61086949..61089441hg38UCSC Ensembl
Outerchr9:43868600..43871100hg19UCSC Ensembl
Cytoband9p11.2
Allele length
AssemblyAllele length
hg382493
hg192501
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1129009
Supporting Variants
SamplesKWS1
Known GenesCNTNAP3B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3961681
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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