A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1069245



Internal ID18970209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:207526954..207569955hg38UCSC Ensembl
chr1:207700299..207743300hg19UCSC Ensembl
Cytoband1q32.2
Allele length
AssemblyAllele length
hg3843002
hg1943002
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3764109
SamplesKWP1
Known GenesCR1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1069245
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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