A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325264



Internal ID20858395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:227107412..227108164hg38UCSC Ensembl
chr1:227295113..227295865hg19UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38753
hg19753
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058191
Samples
Known GenesCDC42BPA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325264
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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