A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353645



Internal ID21011198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:68743895..68750306hg38UCSC Ensembl
chr2:68971027..68977438hg19UCSC Ensembl
Cytoband2p13.3
Allele length
AssemblyAllele length
hg386412
hg196412
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088858
Samples
Known GenesARHGAP25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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