A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772979



Internal ID18958601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12568100..12568801hg38UCSC Ensembl
chr10:12610099..12610800hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068672
Supporting Variants
SamplesKWP1
Known GenesCAMK1D
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772979
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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