A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772638



Internal ID18962178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:226152855..226153118hg38UCSC Ensembl
chr2:227017571..227017834hg19UCSC Ensembl
Cytoband2q36.3
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072075
Supporting Variants
SamplesKWP1
Known GenesLOC646736
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772638
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