A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316196



Internal ID20849274
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:156017848..156028742hg38UCSC Ensembl
chr1:155987639..155998533hg19UCSC Ensembl
Cytoband1q22
Allele length
AssemblyAllele length
hg3810895
hg1910895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18052114
Samples
Known GenesMIR7851, SSR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316196
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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