A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695829



Internal ID15432481
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53721717..53727002hg38UCSC Ensembl
Innerchr7:53789410..53794695hg19UCSC Ensembl
Innerchr7:53756904..53762189hg18UCSC Ensembl
Innerchr7:53563619..53568904hg17UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg385286
hg195286
hg185286
hg175286
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv518399
Supporting Variants
Samples
Known GenesFLJ45974
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695829
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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