A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329330



Internal ID20862482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:77075203..77238980hg38UCSC Ensembl
chr1:77540888..77704665hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38163778
hg19163778
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063187
Samples
Known GenesPIGK
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329330
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer