A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5948409



Internal ID22723892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:151634803..151634803hg38UCSC Ensembl
chrX:150803275..150803275hg19UCSC Ensembl
CytobandXq28
Allele length
AssemblyAllele length
hg38348
hg19348
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17438196
Samples
Known GenesPASD1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5948409
Frequency
Sample Size914
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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