A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017871



Internal ID18760404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:152276772..152485403hg38UCSC Ensembl
Innerchr7:151973857..152182488hg19UCSC Ensembl
Innerchr7:151604790..151813421hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38208632
hg19208632
hg18208632
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674274
Samples
Known GenesFABP5P3, KMT2C, LINC01003
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017871
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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