A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528392



Internal ID15455685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104770826..104826228hg38UCSC Ensembl
Innerchr7:104411273..104466675hg19UCSC Ensembl
Innerchr7:104198509..104253911hg18UCSC Ensembl
Innerchr7:104005224..104060626hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3855403
hg1955403
hg1855403
hg1755403
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv425n21
Supporting Variantsnssv704982
Samples
Known GenesLHFPL3, LHFPL3-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528392
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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