A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337235



Internal ID20994788
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:180764760..180766595hg38UCSC Ensembl
chr2:181629487..181631322hg19UCSC Ensembl
Cytoband2q31.3
Allele length
AssemblyAllele length
hg381836
hg191836
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18081105
Samples
Known GenesSCHLAP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337235
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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