A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6425443



Internal ID21082996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141862204..141886080hg38UCSC Ensembl
chr7:141562004..141585880hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3823877
hg1923877
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150785
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6425443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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