A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518169



Internal ID18816450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27318256..27407511hg38UCSC Ensembl
Innerchr10:27607185..27696440hg19UCSC Ensembl
Innerchr10:27647191..27736446hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3889256
hg1989256
hg1889256
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1049369
Supporting Variants
Samples
Known GenesPTCHD3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518169
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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