A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3518576



Internal ID18470171
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51515226..51540381hg38UCSC Ensembl
Innerchr10:53274986..53300141hg19UCSC Ensembl
Innerchr10:52944992..52970147hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3825156
hg1925156
hg1825156
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1050106
Supporting Variants
Samples
Known GenesPRKG1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3518576
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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