A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6326983



Internal ID20860120
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173567311..173568139hg38UCSC Ensembl
chr1:173536450..173537278hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38829
hg19829
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053125
Samples
Known GenesSLC9C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6326983
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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