A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5976551



Internal ID22751486
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7747365..7762104hg38UCSC Ensembl
chrX:7715406..7730145hg19UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg3814740
hg1914740
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516769
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5976551
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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