A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv522743



Internal ID15450036
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104770826..104846260hg38UCSC Ensembl
Innerchr7:104411273..104486707hg19UCSC Ensembl
Innerchr7:104198509..104273943hg18UCSC Ensembl
Innerchr7:104005224..104080658hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3875435
hg1975435
hg1875435
hg1775435
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv425n21
Supporting Variantsnssv698377
Samples
Known GenesLHFPL3, LHFPL3-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv522743
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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