A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6421587



Internal ID21079140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:154822756..154824935hg38UCSC Ensembl
chr7:154614466..154616645hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg382180
hg192180
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154202
Samples
Known GenesDPP6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6421587
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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