A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5977834



Internal ID22752769
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:72571948..72589683hg38UCSC Ensembl
chrX:71791798..71809533hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3817736
hg1917736
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17516696
Samples
Known GenesHDAC8, PHKA1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5977834
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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