A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12997754



Internal ID6159060
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:146556747..146557723hg38UCSC Ensembl
Innerchr7:146556747..146557723hg38UCSC Ensembl
Outerchr7:146556467..146557966hg38UCSC Ensembl
chr7:146253839..146254815hg19UCSC Ensembl
Innerchr7:146253839..146254815hg19UCSC Ensembl
Outerchr7:146253559..146255058hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38977
hg19977
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3615375
Supporting Variants
SamplesNA19701
Known GenesCNTNAP2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12997754
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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