A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3771470



Internal ID18963502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:102142127..102142728hg38UCSC Ensembl
chrX:101397099..101397700hg19UCSC Ensembl
CytobandXq22.1
Allele length
AssemblyAllele length
hg38602
hg19602
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076269
Supporting Variants
SamplesKWP1
Known GenesTCEAL6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3771470
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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