A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985258



Internal ID12983010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:65424537..65453037hg38UCSC Ensembl
Innerchr7:64889450..64917950hg19UCSC Ensembl
Innerchr7:64526885..64555385hg18UCSC Ensembl
Innerchr7:64333600..64362100hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg3828501
hg1928501
hg1828501
hg1728501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752167
Supporting Variants
SamplesSPC_13
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985258
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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