A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954961



Internal ID17303834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:65866028..65866356hg38UCSC Ensembl
Outerchr18:63533264..63533592hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38329
hg19329
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3002715
SamplesBILGI_BIOE
Known GenesCDH7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954961
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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