A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767818



Internal ID18965875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:24148082..24150883hg38UCSC Ensembl
chrX:24166199..24169000hg19UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg382802
hg192802
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1076250
Supporting Variants
SamplesKWP1
Known GenesZFX, ZFX-AS1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767818
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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