A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820625



Internal ID21265963
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:85254299..85254631hg38UCSC Ensembl
chrX:84509305..84509637hg19UCSC Ensembl
CytobandXq21.1
Allele length
AssemblyAllele length
hg38333
hg19333
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13710736
Samples
Known GenesZNF711
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820625
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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