A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2820344



Internal ID21265682
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:30664039..30664039hg38UCSC Ensembl
chrX:30682156..30682156hg19UCSC Ensembl
CytobandXp21.2
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13697486
Samples
Known GenesGK
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2820344
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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