A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016063



Internal ID19105281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:21700815..21768792hg38UCSC Ensembl
Innerchr7:21740433..21808410hg19UCSC Ensembl
Innerchr7:21706958..21774935hg18UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3867978
hg1967978
hg1867978
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643273
Samples
Known GenesDNAH11
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016063
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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