A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5664629



Internal ID21612934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:54765648..54765712hg38UCSC Ensembl
chrX:54792081..54792145hg19UCSC Ensembl
CytobandXp11.22
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17167489
SamplesHG02587
Known GenesITIH6
MethodMerging
Analysis
PlatformSee merged experiments
Comments
ReferenceEbert_et_al_2021
Pubmed ID33632895
Accession Number(s)nsv5664629
Frequency
Sample Size35
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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