A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6600520



Internal ID20973591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122855439..122855992hg38UCSC Ensembl
chr7:122495493..122496046hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg38554
hg19554
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18149410
Samples
Known GenesCADPS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6600520
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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