A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3512039



Internal ID18810320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27318256..27417672hg38UCSC Ensembl
Innerchr10:27607185..27706601hg19UCSC Ensembl
Innerchr10:27647191..27746607hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3899417
hg1999417
hg1899417
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1044075
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)nssv3512039
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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