A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6606773



Internal ID20979844
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:21494101..21496500hg38UCSC Ensembl
chr7:21533719..21536118hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg382400
hg192400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18156969
Samples
Known GenesSP4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6606773
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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