A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6368120



Internal ID21025673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:30777091..30777488hg38UCSC Ensembl
chr4:30778713..30779110hg19UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg38398
hg19398
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18114774
Samples
Known GenesPCDH7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6368120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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