A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075438



Internal ID18974833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38005027..38005728hg38UCSC Ensembl
chr1:38470699..38471400hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763008
SamplesKWP1
Known GenesFHL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075438
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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