A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009596



Internal ID19098814
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:10566192..10592548hg38UCSC Ensembl
Innerchr1:10626249..10652605hg19UCSC Ensembl
Innerchr1:10548836..10575192hg18UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg3826357
hg1926357
hg1826357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697890
Samples
Known GenesPEX14
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1009596
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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