A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516066



Internal ID15443359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:4395465..4405360hg38UCSC Ensembl
Innerchr10:4437657..4447552hg19UCSC Ensembl
Innerchr10:4427657..4437552hg18UCSC Ensembl
Innerchr10:4427657..4437552hg17UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg389896
hg199896
hg189896
hg179896
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv687438, nssv690787, nssv658317, nssv666939, nssv681113, nssv677354, nssv689030, nssv663462, nssv666430, nssv661737, nssv686698, nssv686595, nssv658634, nssv661487, nssv677666, nssv686631, nssv662309, nssv691010, nssv680462, nssv665985, nssv659465, nssv675156, nssv679186, nssv690149, nssv675922, nssv667116, nssv666545, nssv665965, nssv690064, nssv689658, nssv669369, nssv692701, nssv667242
Samples
Known GenesLINC00703
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516066
Frequency
Sample Size2026
Observed Gain0
Observed Loss33
Observed Complex0
Frequencyn/a


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