A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772369



Internal ID19315632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24313778..24313978hg38UCSC Ensembl
chrX:24331895..24332095hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg38201
hg19201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075721
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772369
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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