A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6324007



Internal ID20857130
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:52440880..52441740hg38UCSC Ensembl
chr1:52906552..52907412hg19UCSC Ensembl
Cytoband1p32.3
Allele length
AssemblyAllele length
hg38861
hg19861
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18061459
Samples
Known GenesZCCHC11
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6324007
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