A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439592



Internal ID21097145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12817547..12835946hg38UCSC Ensembl
chr10:12859546..12877946hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3818400
hg1918401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978841
Samples
Known GenesCAMK1D, LOC283070
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439592
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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