A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032141



Internal ID19121363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:103153042..103196218hg38UCSC Ensembl
Innerchr5:102488746..102531919hg19UCSC Ensembl
Innerchr5:102516645..102559818hg18UCSC Ensembl
Cytoband5q21.1
Allele length
AssemblyAllele length
hg3843177
hg1943174
hg1843174
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5751n100
Supporting Variantsnssv3645911, nssv3645910
Samples
Known GenesPPIP5K2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032141
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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