A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2819232



Internal ID21264570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:70373649..70373720hg38UCSC Ensembl
chrX:69593499..69593570hg19UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3872
hg1972
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv13710456
Samples
Known GenesKIF4A
MethodSequencing
Analysis
Platform
Comments
ReferenceHuddleston_et_al_2016
Pubmed ID27895111
Accession Number(s)nsv2819232
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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