A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6331757



Internal ID20864924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:71144074..71303870hg38UCSC Ensembl
chr1:71609757..71769553hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38159797
hg19159797
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv227n223
Supporting Variantsnssv18062869
Samples
Known GenesZRANB2-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6331757
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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