A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518530



Internal ID15445823
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:7359419..7365372hg38UCSC Ensembl
Innerchr10:7401381..7407334hg19UCSC Ensembl
Innerchr10:7441387..7447340hg18UCSC Ensembl
Innerchr10:7441387..7447340hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg385954
hg195954
hg185954
hg175954
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695973
Samples
Known GenesSFMBT2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518530
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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