A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340317



Internal ID20997870
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:164566745..164574418hg38UCSC Ensembl
chr2:165423255..165430928hg19UCSC Ensembl
Cytoband2q24.3
Allele length
AssemblyAllele length
hg387674
hg197674
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079696
Samples
Known GenesGRB14
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340317
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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