A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024237



Internal ID18766770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140810775..140852242hg38UCSC Ensembl
Innerchr5:140190360..140231827hg19UCSC Ensembl
Innerchr5:140170544..140212011hg18UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3841468
hg1941468
hg1841468
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3648143
Samples
Known GenesPCDHA1, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1024237
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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