A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764574



Internal ID19308756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:110816971..110822072hg38UCSC Ensembl
chrX:110060199..110065300hg19UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg385102
hg195102
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1078680
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764574
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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