A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5974962



Internal ID22749897
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:13907722..13908721hg38UCSC Ensembl
chrX:13925841..13926840hg19UCSC Ensembl
CytobandXp22.2
Allele length
AssemblyAllele length
hg381000
hg191000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17515502
Samples
Known GenesGPM6B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5974962
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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