A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14435893



Internal ID22179004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:134920257..134920346hg38UCSC Ensembl
chr7:134605008..134605097hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3890
hg1990
Variant TypeOTHER complex substitution
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3189104
Supporting Variants
SamplesHG00514
Known GenesCALD1
MethodMerging
AnalysisPhasedSV,MsPAC, Multiple Illumina callers, BioNano Genomics software
PlatformSee merged experiments
Comments
ReferenceChaisson_et_al_2019
Pubmed ID30992455
Accession Number(s)nssv14435893
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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