A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029547



Internal ID19118766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:61081237..61306083hg38UCSC Ensembl
Innerchr7:61063962..61288808hg19UCSC Ensembl
Innerchr7:61067904..61292750hg18UCSC Ensembl
Cytoband7q11.1
Allele length
AssemblyAllele length
hg38224847
hg19224847
hg18224847
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661532
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029547
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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