A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031777



Internal ID19120999
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7167547..7202707hg38UCSC Ensembl
Innerchr5:7167660..7202820hg19UCSC Ensembl
Innerchr5:7220660..7255820hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3835161
hg1935161
hg1835161
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5559n100
Supporting Variantsnssv3746182
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)nsv1031777
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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