A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012289



Internal ID19101507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:7360231..7393565hg38UCSC Ensembl
Innerchr4:7361958..7395292hg19UCSC Ensembl
Innerchr4:7412859..7446193hg18UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3833335
hg1933335
hg1833335
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3616186
Samples
Known GenesSORCS2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012289
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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