A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12738673



Internal ID5584632
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37731290..37853637hg38UCSC Ensembl
chr7:37770892..37893239hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38122348
hg19122348
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3612860
Supporting Variants
SamplesNA19025
Known GenesGPR141, NME8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12738673
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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