A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075305



Internal ID18970177
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:3691429..3691485hg38UCSC Ensembl
chrX:3609470..3609526hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg3857
hg1957
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3763305
SamplesKWP1
Known GenesPRKX
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075305
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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