A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764151



Internal ID18968917
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:205816254..205834810hg38UCSC Ensembl
chr1:205785382..205803938hg19UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg3818557
hg1918557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1069227
Supporting Variants
SamplesKWP1
Known GenesPM20D1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764151
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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