A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525011



Internal ID15452304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:3156700..3225096hg38UCSC Ensembl
Innerchr7:3196333..3264728hg19UCSC Ensembl
Innerchr7:3162859..3231254hg18UCSC Ensembl
Innerchr7:2969574..3037969hg17UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3868397
hg1968396
hg1868396
hg1768396
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701048
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525011
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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