A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044106



Internal ID18786637
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:3136689..3186881hg38UCSC Ensembl
Innerchr10:3178881..3229073hg19UCSC Ensembl
Innerchr10:3168881..3219073hg18UCSC Ensembl
Cytoband10p15.2
Allele length
AssemblyAllele length
hg3850193
hg1950193
hg1850193
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3500027
Samples
Known GenesPFKP, PITRM1, PITRM1-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044106
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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