A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14436295



Internal ID22179430
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7207479..7207530hg38UCSC Ensembl
chr10:7249441..7249492hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3852
hg1952
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3226532
Supporting Variants
SamplesHG00514
Known GenesSFMBT2
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14436295
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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