A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6317788



Internal ID20850877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:75882632..75924160hg38UCSC Ensembl
chr1:76348317..76389845hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3841529
hg1941529
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064069
Samples
Known GenesASB17, MSH4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6317788
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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