A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1075334



Internal ID18975297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140503434..140504335hg38UCSC Ensembl
chrX:139585599..139586500hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3765002
SamplesKWP1
Known GenesSOX3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1075334
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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