A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525378



Internal ID15452671
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:25566105..25575601hg38UCSC Ensembl
Innerchr7:25605725..25615221hg19UCSC Ensembl
Innerchr7:25572250..25581746hg18UCSC Ensembl
Innerchr7:25378965..25388461hg17UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg389497
hg199497
hg189497
hg179497
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv417n21
Supporting Variantsnssv701499
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525378
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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