A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9839037



Internal ID1564895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:777664..820586hg38UCSC Ensembl
chr1:713044..755966hg19UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3842923
hg1942923
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3584977
Supporting Variants
SamplesHG01444
Known GenesFAM87B, LOC100288069
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9839037
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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