A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325219



Internal ID20858350
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173574601..173580200hg38UCSC Ensembl
chr1:173543740..173549339hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg385600
hg195600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053126
Samples
Known GenesSLC9C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325219
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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