A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3506012



Internal ID18804293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:130058109..130097459hg38UCSC Ensembl
Innerchr10:131856373..131895723hg19UCSC Ensembl
Innerchr10:131746363..131785713hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3839351
hg1939351
hg1839351
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039523
Supporting Variants
Samples
Known GenesLINC00959
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3506012
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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