A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697566



Internal ID18649161
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 StatusS
Merged Variantsnsv1053762
Supporting Variants
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)nssv3697566
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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