A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12995156



Internal ID2747488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:144892010..144892908hg38UCSC Ensembl
Innerchr7:144892023..144892896hg38UCSC Ensembl
Outerchr7:144891998..144892921hg38UCSC Ensembl
chr7:144589103..144590001hg19UCSC Ensembl
Innerchr7:144589116..144589989hg19UCSC Ensembl
Outerchr7:144589091..144590014hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38899
hg19899
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615325
Supporting Variants
SamplesHG02410
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12995156
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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