A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3500027



Internal ID18740982
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 StatusS
Merged Variantsnsv1044106
Supporting Variants
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)nssv3500027
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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