A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456761



Internal ID21114314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:62577264..62577912hg38UCSC Ensembl
chr12:62971044..62971692hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg38649
hg19649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18002105
Samples
Known GenesMON2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456761
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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