A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353065



Internal ID21010618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180807144..180821442hg38UCSC Ensembl
chr2:181671871..181686169hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg3814299
hg1914299
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081115
Samples
Known GenesSCHLAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353065
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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