A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18125199



Internal ID20692239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:140927337..140937328hg38UCSC Ensembl
chr5:140306922..140316913hg19UCSC Ensembl
Cytoband5q31.3
Allele length
AssemblyAllele length
hg389992
hg199992
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404446
Supporting Variants
Samples
Known GenesPCDHA1, PCDHA10, PCDHA11, PCDHA12, PCDHA13, PCDHA2, PCDHA3, PCDHA4, PCDHA5, PCDHA6, PCDHA7, PCDHA8, PCDHA9, PCDHAC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18125199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.0001


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