A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv677432



Internal ID15414084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89905292..90209393hg38UCSC Ensembl
Innerchr7:89534606..89838707hg19UCSC Ensembl
Innerchr7:89372542..89676643hg18UCSC Ensembl
Innerchr7:89179257..89483358hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38304102
hg19304102
hg18304102
hg17304102
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515997
Supporting Variants
Samples
Known GenesDPY19L2P4, STEAP1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv677432
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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