A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770782



Internal ID18959349
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:62686191..62686518hg38UCSC Ensembl
chr1:63151862..63152189hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076485
Supporting Variants
SamplesKWP1
Known GenesDOCK7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770782
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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