A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772964



Internal ID19305709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:65865964..65866350hg38UCSC Ensembl
chr18:63533200..63533586hg19UCSC Ensembl
Cytoband18q22.1
Allele length
AssemblyAllele length
hg38387
hg19387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1071856
Supporting Variants
SamplesKWP1
Known GenesCDH7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772964
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