A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075812



Internal ID19315756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32964098..32964699hg38UCSC Ensembl
chr1:33429699..33430300hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3769467
SamplesKWP1
Known GenesRNF19B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075812
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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