A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv483124



Internal ID15582237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:87026523..87173407hg38UCSC Ensembl
Innerchr7:86655839..86802723hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38146885
hg19146885
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2995915
Samples
Known GenesDMTF1, KIAA1324L
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nsv483124
Frequency
Sample Size39
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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