A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766144



Internal ID18966417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25287608..25335109hg38UCSC Ensembl
chr1:25614099..25661600hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3847502
hg1947502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077264
Supporting Variants
SamplesKWP1
Known GenesRHD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766144
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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