A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953706



Internal ID17302580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
OuterchrX:151911729..151924628hg38UCSC Ensembl
OuterchrX:151080201..151093100hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg3812900
hg1912900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000319
SamplesBILGI_BIOE
Known GenesMAGEA4
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953706
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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