A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077216



Internal ID19316434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:1637106..1641407hg38UCSC Ensembl
chrX:1755999..1760300hg19UCSC Ensembl
CytobandXp22.33
Allele length
AssemblyAllele length
hg384302
hg194302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3770284
SamplesKWP1
Known GenesASMT
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077216
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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