A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030062



Internal ID19119281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:18876251..18903786hg38UCSC Ensembl
Innerchr7:18915874..18943409hg19UCSC Ensembl
Innerchr7:18882399..18909934hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3827536
hg1927536
hg1827536
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643235
Samples
Known GenesHDAC9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030062
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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