A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017793



Internal ID19107010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:55983574..56030337hg38UCSC Ensembl
Innerchr7:56051267..56098030hg19UCSC Ensembl
Innerchr7:56018761..56065524hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3846764
hg1946764
hg1846764
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661424
Samples
Known GenesGBAS, PSPH
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017793
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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