A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432625



Internal ID21090178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:157611191..157616696hg38UCSC Ensembl
chr7:157403883..157409388hg19UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg385506
hg195506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18151541
Samples
Known GenesPTPRN2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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