A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607645



Internal ID20980716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:151297001..151302600hg38UCSC Ensembl
chr6:151618136..151623735hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18141479
Samples
Known GenesAKAP12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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