A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6334509



Internal ID20867696
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:173597597..173598412hg38UCSC Ensembl
chr1:173566736..173567551hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg38816
hg19816
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18053132
Samples
Known GenesSLC9C2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6334509
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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