A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601670



Internal ID20974741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:123502801..123504000hg38UCSC Ensembl
chr7:123142855..123144054hg19UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150075
Samples
Known GenesIQUB
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601670
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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