A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374693



Internal ID21032246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71376262..71379537hg38UCSC Ensembl
chr3:71425413..71428688hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383276
hg193276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18103750
Samples
Known GenesFOXP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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