A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430770



Internal ID21088323
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:141020501..141025600hg38UCSC Ensembl
chr7:140720301..140725400hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18150732
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430770
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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