A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv482984



Internal ID15582352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:133676624..133855751hg38UCSC Ensembl
Innerchr9:136541746..136720873hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg38179128
hg19179128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2996443
Samples
Known GenesSARDH, VAV2
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv482984
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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