A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687306



Internal ID15423958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:45653..67820hg38UCSC Ensembl
Innerchr7:45653..67820hg19UCSC Ensembl
Innerchr7:140736..162903hg18UCSC Ensembl
Innerchr7:140736..162903hg17UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3822168
hg1922168
hg1822168
hg1722168
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516015
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687306
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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