A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6601552



Internal ID20974623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:1587396..1608961hg38UCSC Ensembl
chr7:1627032..1648597hg19UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg3821566
hg1921566
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152190
Samples
Known GenesPSMG3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6601552
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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