A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515466



Internal ID22573427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:136247268..136254268hg38UCSC Ensembl
chrX:135329427..135336427hg19UCSC Ensembl
CytobandXq26.3
Allele length
AssemblyAllele length
hg387001
hg197001
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5970720
Supporting Variants
Samples
Known GenesMAP7D3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515466
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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