A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3525740



Internal ID22395118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136033603..136033662hg38UCSC Ensembl
chrX:135115762..135115821hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14354334, nssv14354335
SamplesHG00731, HG00733
Known GenesSLC9A6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nsv3525740
Frequency
Sample Size9
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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