A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819771



Internal ID21265109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:120374826..120374826hg38UCSC Ensembl
chrX:119508681..119508681hg19UCSC Ensembl
CytobandXq24
Allele length
AssemblyAllele length
hg38100
hg19100
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13711351
Samples
Known GenesATP1B4
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819771
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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