A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3770818



Internal ID18961369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:152118027..152119528hg38UCSC Ensembl
chrX:151286499..151288000hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg381502
hg191502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075342
Supporting Variants
SamplesKWP1
Known GenesMAGEA10-MAGEA5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3770818
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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