A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321571



Internal ID20854678
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:155045696..155071730hg38UCSC Ensembl
chr1:155018172..155044206hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3826035
hg1926035
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052054
Samples
Known GenesADAM15, DCST1, EFNA4, LOC100505666
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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