A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3526958



Internal ID22396342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120463731..120463957hg38UCSC Ensembl
chrX:119597586..119597812hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38227
hg19227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14352723, nssv14352722
SamplesHG00513, HG00514
Known GenesLAMP2
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3526958
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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