A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6430730



Internal ID21088283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:130954464..130958036hg38UCSC Ensembl
chr7:130639223..130642795hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg383573
hg193573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18154064
Samples
Known GenesLINC-PINT
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6430730
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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