A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1156388



Internal ID22086789
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 Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4020220, nssv4020229, nssv4020221, nssv4020231, nssv4020219, nssv4020223, nssv4020224, nssv4020222, nssv4020227, nssv4020230, nssv4020232, nssv4020226, nssv4020225, nssv4020228
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)nsv1156388
Frequency
Sample Size131
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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