A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026359



Internal ID18768891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:181005..231133hg38UCSC Ensembl
Innerchr7:181005..231133hg19UCSC Ensembl
Innerchr7:276088..326216hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3850129
hg1950129
hg1850129
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3752783, nssv3654220
Samples
Known GenesFAM20C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026359
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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