A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14331847



Internal ID22262549
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:14318613..14324114hg38UCSC Ensembl
chr10:14360612..14366113hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385502
hg195502
Variant TypeCNV deletion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3220571
Supporting Variants
SamplesNA19238
Known GenesFRMD4A
MethodSequencing
AnalysisMultiple analysis algorthms
PlatformIllumina HiSeq
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14331847
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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