A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3671096



Internal ID18622691
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143773034..143897882hg38UCSC Ensembl
Innerchr7:143470127..143594975hg19UCSC Ensembl
Innerchr7:143101060..143225908hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38124849
hg19124849
hg18124849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1023202
Supporting Variants
Samples
Known GenesFAM115A, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3671096
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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