A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763154



Internal ID19307283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1404806..1407607hg38UCSC Ensembl
chrX:1523699..1526500hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076695
Supporting Variants
SamplesKWP1
Known GenesASMTL, ASMTL-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763154
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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