A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3517555



Internal ID18815836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27321149..27417672hg38UCSC Ensembl
Innerchr10:27610078..27706601hg19UCSC Ensembl
Innerchr10:27650084..27746607hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3896524
hg1996524
hg1896524
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1045904
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)nssv3517555
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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