A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4020229



Internal ID22081860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:140844251..140864171hg38UCSC Ensembl
Outerchr5:140839137..140872578hg38UCSC Ensembl
Innerchr5:140223836..140243756hg19UCSC Ensembl
Outerchr5:140218722..140252163hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg3833442
hg1933442
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1156388
Supporting Variants
Samples
Known GenesPCDHA1, PCDHA10, PCDHA11, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)nssv4020229
Frequency
Sample Size131
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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