A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820907



Internal ID21266245
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:76034023..76034332hg38UCSC Ensembl
chrX:75253858..75254167hg19UCSC Ensembl
CytobandXq13.3
Allele length
AssemblyAllele length
hg38310
hg19310
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13703004
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820907
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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