A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1049772



Internal ID19138991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:27329276..27413580hg38UCSC Ensembl
Innerchr10:27618205..27702509hg19UCSC Ensembl
Innerchr10:27658211..27742515hg18UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg3884305
hg1984305
hg1884305
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv696n100
Supporting Variantsnssv3512233
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)nsv1049772
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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