A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765673



Internal ID18960735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:119103587..119104588hg38UCSC Ensembl
chr10:120863099..120864100hg19UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg381002
hg191002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070894
Supporting Variants
SamplesKWP1
Known GenesFAM45A, FAM45B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765673
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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