A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv662440



Internal ID15399092
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62551843..62654636hg38UCSC Ensembl
Innerchr7:62012221..62115014hg19UCSC Ensembl
Innerchr7:61649656..61752449hg18UCSC Ensembl
Innerchr7:61456371..61559164hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38102794
hg19102794
hg18102794
hg17102794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516283
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv662440
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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