A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028065



Internal ID18770596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143780203..143875193hg38UCSC Ensembl
Innerchr7:143477296..143572286hg19UCSC Ensembl
Innerchr7:143108229..143203219hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3894991
hg1994991
hg1894991
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6718n100
Supporting Variantsnssv3671124
Samples
Known GenesFAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028065
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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