A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12997575



Internal ID6907278
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145924728..145928370hg38UCSC Ensembl
Innerchr7:145924733..145928365hg38UCSC Ensembl
Outerchr7:145924723..145928375hg38UCSC Ensembl
chr7:145621821..145625463hg19UCSC Ensembl
Innerchr7:145621826..145625458hg19UCSC Ensembl
Outerchr7:145621816..145625468hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg383643
hg193643
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615360
Supporting Variants
SamplesNA21112
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12997575
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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