A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077230



Internal ID18977101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:47221400..47223201hg38UCSC Ensembl
chrX:47080799..47082600hg19UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg381802
hg191802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3766025
SamplesKWP1
Known GenesCDK16
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077230
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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