A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1053762



Internal ID18796293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:95446260..95469838hg38UCSC Ensembl
Innerchr9:98208542..98232120hg19UCSC Ensembl
Innerchr9:97248363..97271941hg18UCSC Ensembl
Cytoband9q22.32
Allele length
AssemblyAllele length
hg3823579
hg1923579
hg1823579
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697566
Samples
Known GenesLOC100507346, PTCH1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1053762
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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