A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6318622



Internal ID20851714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:1970523..1972865hg38UCSC Ensembl
chr1:1901962..1904304hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg382343
hg192343
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18056365
Samples
Known GenesKIAA1751
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6318622
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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