A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077011



Internal ID19324497
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:7770377..7771478hg38UCSC Ensembl
chr8:7627899..7629000hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770288
SamplesKWP1
Known GenesFAM90A10P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077011
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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