A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412642



Internal ID21070195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:10695097..10696037hg38UCSC Ensembl
chr6:10695330..10696270hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38941
hg19941
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136904
Samples
Known GenesPAK1IP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412642
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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