A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14354334



Internal ID22195344
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3525740
Supporting Variants
SamplesHG00731
Known GenesSLC9A6
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14354334
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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