A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766667



Internal ID18959132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:19467693..19467756hg38UCSC Ensembl
chrX:19485811..19485874hg19UCSC Ensembl
CytobandXp22.12
Allele length
AssemblyAllele length
hg3864
hg1964
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076247
Supporting Variants
SamplesKWP1
Known GenesMAP3K15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766667
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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