A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3697890



Internal ID18996171
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 StatusS
Merged Variantsnsv1009596
Supporting Variants
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)nssv3697890
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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