A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987734



Internal ID12981395
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:74363164..74419664hg38UCSC Ensembl
Innerchr6:75072880..75129380hg19UCSC Ensembl
Innerchr6:75129600..75186100hg18UCSC Ensembl
Innerchr6:75129600..75186100hg17UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg3856501
hg1956501
hg1856501
hg1756501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv35015
Supporting Variants
SamplesNA18967
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987734
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer