A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6424212



Internal ID21081765
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:137212201..137214000hg38UCSC Ensembl
chr7:136896948..136898747hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg381800
hg191800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6424212
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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