A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767760



Internal ID19306944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:105380544..105380699hg38UCSC Ensembl
chr8:106392772..106392927hg19UCSC Ensembl
Cytoband8q23.1
Allele length
AssemblyAllele length
hg38156
hg19156
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075572
Supporting Variants
SamplesKWP1
Known GenesZFPM2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767760
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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