A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025665



Internal ID19114883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7177225..7204503hg38UCSC Ensembl
Innerchr5:7177338..7204616hg19UCSC Ensembl
Innerchr5:7230338..7257616hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3827279
hg1927279
hg1827279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5559n100
Supporting Variantsnssv3639628
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1025665
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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