A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819857



Internal ID21265195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:18881549..18881602hg38UCSC Ensembl
chrX:18899667..18899720hg19UCSC Ensembl
CytobandXp22.13
Allele length
AssemblyAllele length
hg3854
hg1954
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13706338
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819857
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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