A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021852



Internal ID19111070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:7148262..7189812hg38UCSC Ensembl
Innerchr5:7148375..7189925hg19UCSC Ensembl
Innerchr5:7201375..7242925hg18UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg3841551
hg1941551
hg1841551
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3638602
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)nsv1021852
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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