A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770183



Internal ID19313769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64340981..64341301hg38UCSC Ensembl
chr15:64633180..64633500hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg38321
hg19321
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069593
Supporting Variants
SamplesKWP1
Known GenesCSNK1G1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770183
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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