A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700940



Internal ID15090906
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:141972804..141986383hg38UCSC Ensembl
Innerchr7:141672604..141686183hg19UCSC Ensembl
Innerchr7:141319073..141332652hg18UCSC Ensembl
Innerchr7:141125788..141139367hg17UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3813580
hg1913580
hg1813580
hg1713580
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524927
Supporting Variants
Samples
Known GenesTAS2R38
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700940
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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