A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019979



Internal ID19109198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:160920605..160936446hg38UCSC Ensembl
Innerchr5:160347612..160363453hg19UCSC Ensembl
Innerchr5:160280190..160296031hg18UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3815842
hg1915842
hg1815842
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648229
Samples
Known GenesLOC285629
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1019979
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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