A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524487



Internal ID15105094
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28957328..28959047hg38UCSC Ensembl
Innerchr7:28996944..28998663hg19UCSC Ensembl
Innerchr7:28963469..28965188hg18UCSC Ensembl
Innerchr7:28770184..28771903hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381720
hg191720
hg181720
hg171720
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700425
Samples
Known GenesTRIL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524487
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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