A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1072638



Internal ID19319386
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:38382645..38387482hg38UCSC Ensembl
chr22:38778650..38783487hg19UCSC Ensembl
Cytoband22q13.1
Allele length
AssemblyAllele length
hg384838
hg194838
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3772160
SamplesKWP1
Known GenesLOC400927
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1072638
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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