A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2765901



Internal ID17508033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:66319976..66325660hg38UCSC Ensembl
Innerchr13:66894108..66899792hg19UCSC Ensembl
Innerchr13:65792109..65797793hg18UCSC Ensembl
Cytoband13q21.32
Allele length
AssemblyAllele length
hg385685
hg195685
hg185685
Variant TypeCNV deletion
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv976260
Supporting Variants
SamplesHGDP01029
Known GenesPCDH9
MethodSequencing
AnalysisHuman CNVs
PlatformNot reported
Comments
ReferenceSudmant_et_al_2013
Pubmed ID23825009
Accession Number(s)nssv2765901
Frequency
Sample Size10
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer