A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17515529



Internal ID22573491
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:140690698..140712905hg38UCSC Ensembl
chrX:139772863..139795070hg19UCSC Ensembl
CytobandXq27.1
Allele length
AssemblyAllele length
hg3822208
hg1922208
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976139
Supporting Variants
Samples
Known GenesLINC00632
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17515529
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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