A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv15752197



Internal ID21386221
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr14:61762456..61763486hg38UCSC Ensembl
chr14:62229174..62230204hg19UCSC Ensembl
Cytoband14q23.2
Allele length
AssemblyAllele length
hg381031
hg191031
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4432121
Supporting Variants
SamplesMDQ010
Known GenesSNAPC1
MethodSequencing
Analysis
Platform
Comments
ReferenceDeng_et_al_2019
Pubmed ID31718558
Accession Number(s)nssv15752197
Frequency
Sample Size15
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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