A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515822



Internal ID15096429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:113090435..113104996hg38UCSC Ensembl
Innerchr9:115852715..115867276hg19UCSC Ensembl
Innerchr9:114892536..114907097hg18UCSC Ensembl
Innerchr9:112932269..112946830hg17UCSC Ensembl
Cytoband9q32
Allele length
AssemblyAllele length
hg3814562
hg1914562
hg1814562
hg1714562
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv683659, nssv685701, nssv689011, nssv671249, nssv680579, nssv662338, nssv686967, nssv690087, nssv655746, nssv657332, nssv682010, nssv661213, nssv692342, nssv664886, nssv686541, nssv674886, nssv692138, nssv680026
Samples
Known GenesFAM225B
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515822
Frequency
Sample Size2026
Observed Gain0
Observed Loss18
Observed Complex0
Frequencyn/a


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