A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077264



Internal ID18969779
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 StatusM
Merged Variants
Supporting Variantsnssv3766144
SamplesKWP1
Known GenesRHD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077264
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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